Create a Report
Please provide report title
Please provide location
Please provide details
Get alerts and updates for your case! Your contact information is not shown on the website.
This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.
Please provide email or phone
Please provide email or phone

We do not show your email or contact info

Please accept our Terms & Conditions
Add photos or video
We recommend photos and videos to help explain your report
Add Photo/Video
Email or SMS copy of report
Enter below to get emailed a copy of your report, or sms a link to your report
Please provide email or phone
Please provide email or phone
Please accept our Terms & Conditions
Thank you for your report!


IMPORTANT - Your report is queued
It may take up to 12 hours to process your report.


Email us at support@safelyhq.com if you have questions.

Please provide location
Please provide location
Please provide report title
Please provide details
Please accept our Terms & Conditions
Get alerts and updates for your case! Your contact information is not shown on the website.

This information is not shown on the website. We can notify you of updates, and may contact you for more information to help resolve or follow up on your issue.

or
Please provide email or phone
Thank you for your report!

IMPORTANT - YOUR REPORT IS QUEUED - IT MAY TAKE UP TO 12 HOURS FOR YOUR REPORT TO SHOW ON OUR HOME PAGE (IF NOT OPTED AS PRIVATE)

Visit our learn pages for more helpful information or, email us: support@safelyhq.com

Goodbye! and best wishes in your recovery

Oscor Destino Twist & Guidestar - recalled due to potential detachment, USA

6 months ago

United States

Oscor Inc. is voluntarily recalling 14 lots of Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 down to the user level. The Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 have been found to have increased risk of the hub cap and seal on the proximal end of the device handle detaching during use.

RISK STATEMENT: The Destino Twist 14T Model DST1405525 & Guidestar 14F Model D141103 detachment of the hub cap and seal could lead to bleeding at the proximal end of the device and/or air embolism for the patient during intracardiac, renal or other peripheral placements procedures.

Oscor Inc. has reported two (2) Medical Device Reports to the FDA related to detachment of hub cap and seal on the proximal end of the device handle. The recall is limited to the two model numbers and lot numbers outlined above. There are no other recalls associated with this product.

PRODUCT INFORMATION: The product is steerable guiding sheath intended for the introduction of diagnostic and therapeutic devices into the human vascular, including but not limited to intracardiac, renal or other peripheral placements; it cannot be use for neural placements. The product is provided sterile, one unit per pouch / tray for details and can be identified on the printed labeling with the information below (1, 2, and 3).

The affected Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 were distributed Worldwide to distributors and hospitals from June 8, 2021 to November 30, 2021.

Recalled Product Impacted (1)

- Destino Twist 14F (DST1405525). UDI Number: 885672011123. Lot Number: PQOC13475. Expiration Date 10-01-2021. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP14073. Expiration Date 11-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP14072. Expiration Date 10-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP14071. Expiration Date 10-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP13834. Expiration Date 09-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP13828. Expiration Date 09-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: DP13827. Expiration Date 08-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12995. Expiration Date 07-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12632. Expiration Date 07-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12633. Expiration Date 07-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12345. Expiration Date 06-01-2024. Packaging State Type: Sterile.
- Guidestar 14F (D141103). UDI Number: 885692010911. Lot Number: PQOC12330. Expiration Date 06-01-2025. Packaging State Type: Sterile.

Destino 14F Twist Model (2)

Product: Destino Twist 14F
GTIN (Unit): 00885672011123
Model: DST1405525
Sheath & Dilator: S55CM D73CM
French Size: 14F
Quantity: 6 Units

Guidestar 14F - Model (3)

Product: Guidestar 14F
GTIN (Unit): 00885672010911
Model: D141103
Sheath & Dilator: S71CM D89CM
French Size: 14F
Quantity: 543 Units

Company name: Oscor Inc.
Brand name: Oscor
Recalled: Destino Twist 14F model DST1405525 & Guidestar 14F model D141103 steerable guiding sheath
Reason of the recall: Hub cap and seal on the proximal end of the device handle may detach during use
FDA Recall date: January 12, 2022

Check the full recall details on fda.gov

Source: FDA

458


Related Reports

Edgewell Personal Care Company (NYSE: EPC) today issued a voluntary nationwide recall of three batches of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 to the consumer level as outlined in the list below. An internal review found that some samples of the product contained trace... See More levels of benzene. While benzene is not an ingredient in any Banana Boat products, the review showed that unexpected levels of benzene came from the propellant that sprays the product out of the can. To date, Edgewell has not received any adverse events related to this recall. The products were distributed nationwide in the United States through various retailers and online. Edgewell has notified its retailers to remove any remaining recalled product from shelves.

Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it potentially can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life threatening. Benzene is ubiquitous in the environment. Humans around the world have daily exposures to it indoors and outdoors from multiple sources. Daily exposure to benzene in the recalled products would not be expected to cause adverse health consequences according to an independent health assessment using established exposure modeling guidelines.

Importantly, no other batches of Hair & Scalp (either before or after these batch codes) and no other Banana Boat products are in the scope of this recall and may continue to be used by consumers safely and as intended.

UPC: 0-79656-04041-8, DESCRIPTION: Banana Boat Hair & Scalp Spray SPF 30, Lot Code: 20016AF, Expiration: December 2022, Size: 6 oz
UPC: 0-79656-04041-8, DESCRIPTION: Banana Boat Hair & Scalp Spray SPF 30, Lot Code: 20084BF, Expiration: February 2023, Size: 6 oz
UPC: 0-79656-04041-8, DESCRIPTION: Banana Boat Hair & Scalp Spray SPF 30, Lot Code: 21139AF, Expiration: April 2024, Size: 6 oz

The voluntarily recalled sunscreen spray products are packaged in aerosol cans. Banana Boat will also offer reimbursement for consumers who have purchased a product marked with one of the lot codes in the table above. Lot codes are located on the bottom of the can. Consumers should stop using the affected product immediately and appropriately discard.

In case you experienced harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Edgewell Personal Care Company
Brand name: Banana Boat
Product recalled: Hair & scalp sunscreen spray
Reason of the recall: Due to presence of benzene
FDA Recall date: July 29, 2022

Source: fda.gov
See Less
459


DISTRIBUTOR RFR, LLC. is voluntarily recalling lot #48656, Exp. 01/2025 of SANGTER Energy Supplement, 3000 mg, packaged in 7-count blister packs within a carton to the consumer level. FDA analysis has found the product to contain undeclared sildenafil. Sildenafil is a phosphodiesterase (PDE-5) inhibitor found in FDA-approved... See More products for the treatment of male erectile dysfunction. The presence of sildenafil in SANGTER makes it an unapproved new drug for which the safety and efficacy has not been established and, therefore subject to recall. To date, DISTRIBUTOR RFR, LLC. has not received any reports of adverse events related to this recall.

The tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in a 7-count blister pack within a carton, UPC 0 705632 523285, and was distributed through retail stores in the state of Florida from 02/01/2002 to 07/20/2022 and Nationwide in the USA through our website from 02/01/2002 to 07/20/2022  www.sangter.com.

Distributor RFR, LLC is notifying its distributors and customers through this notice and is arranging for the return of all recalled products. All customers are urged to stop consuming the product marked with this lot, and to contact their physician or health care provider if they have experienced any problems that may be related to taking or using this medication.

Risk Statement: Use of SANGTER with undeclared sildenafil may pose a threat to consumers because it may interact with nitrates found in some prescription drugs (such as nitroglycerin) and may cause a significant drop in blood pressure that may be life threatening. People with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates. Among the adult male population who are most likely to use these products, adult males who use nitrates for cardiac conditions are at the most at risk from these products.

Company name: Distributor RFR, LLC
Brand name: SANGTER
Product recalled: SANGTER Energy Supplement, 3000mg
Reason of the recall: Undeclared Sildenafil
FDA Recall date: August 02, 2022

Source: fda.gov
See Less
458


Plastikon Healthcare, LLC is issuing an update to the voluntary recall initiated on June 3, 2022.  The recall has been expanded to include Lot 20076A of Magnesium Hydroxide 1200 mg / Aluminum Hydroxide 1200 mg / Simethicone 120 mg per 30 mL Oral Suspension. The products are... See More being recalled due to microbial contamination. To date, Plastikon Healthcare has not received any reports of adverse events or injuries related to this recall.

This lot was previously subject to a retail level recall and has been added to the current consumer level recall based on updated microorganism speciation data from third-party testing. The updated recall includes one (1) lot of Milk of Magnesia 2400 mg/10 mL Oral Suspension, one (1) lot of Milk of Magnesia 2400 mg/30 mL Oral Suspension, twelve (12) lots of Magnesium Hydroxide 1200 mg/Aluminum Hydroxide 1200 mg/Simethicone 120 mg per 30 mL Oral Suspension, and two (2) lots of Magnesium Hydroxide 2400 mg/Aluminum Hydroxide 2400 mg/Simethicone 240 mg per 30 mL Oral Suspension to the consumer level. 

Risk Statement: Administration or use of drug products with microbial contamination could potentially result in increased infections that may require medical intervention.  Patients with compromised immune systems, such as patients in hospitals and nursing homes, have a higher probability of developing potentially life-threatening infections after taking a contaminated product. 

Product indication, lot numbers, expiration dates, and NDC information are listed below. The products are packaged for institutional use and are sold to clinics and hospitals nationwide in single use cups with a foil lid.  The affected lots were distributed to Major Pharmaceuticals Distribution Center (wholesaler) between 7/1/2020 and 10/31/2021, who shipped to hospitals, nursing homes, and clinics nationwide.  The products are private labeled for Major Pharmaceuticals.

Product Name: Milk of Magnesia, 2400 mg / 30 mL, Oral Suspension.
Indications for Use: Occasional relief of constipation, (irregularity) in adults and children 12 years and older or for children under 12 as recommended by a doctor.
Lot/Exp: 20071A / Jul. 2022
NDC: 0904-6846-73
Packaging: Carton containing, 100 single dose cups (10 trays x 10 cups).

Product Name: Milk of Magnesia, 2400 mg / 10 mL, Oral Suspension.
Indications for Use: Occasional relief of constipation, (irregularity) in adults and children 12 years and older or for children under 12 as recommended by a doctor.
Lot/Exp: 20074A / Jul. 2022
NDC: 0904-6840-72
Packaging: Carton containing, 100 single dose cups (10 trays x 10 cups).

Product Name: Magnesium, Hydroxide 1200 mg / Aluminum, Hydroxide 1200 mg/ Simethicone 120 mg per 30 mL Oral Suspension.
Indications for Use: Relief of acid indigestion, heartburn, sour stomach, upset stomach due to these symptoms, pressure and bloating
commonly referred to as gas.
Lot/Exp: 21103A / Sep. 2023, 20046A / May 2022, 20076A / Jul. 2022, 20079A / Aug. 2022, 20080A / Aug. 2022, 20081A / Aug. 2022, 21057A / May 2023, 21059A / May 2023, 21095A / Sep. 2023, 21096A / Sep. 2023, 21099A / Sep. 2023, 21115A / Oct. 2022
NDC: 0904-6838-73
Packaging: Carton containing 100 single dose cups (10 trays x 10 cups).

Product Name: Magnesium Hydroxide 2400 mg / Aluminum, Hydroxide 2400 mg / Simethicone, 240 mg per 30 mL Oral Suspension.
Indications for Use: Relief of acid indigestion, heartburn, sour stomach, upset stomach due to these symptoms, pressure and bloating
commonly referred to as gas.
Lot/Exp: 20051A / Aug. 2022, 20088A / Sep. 2022
NDC: 0904-6839-73
Packaging: Carton containing 100 single dose cups (10 trays x 10 cups).

Company name: Plastikon Healthcare, LLC
Brand name: Major
Product recalled: Milk of Magnesia, Magnisium Hydroxide/Aluminum Hydroxide/Simethicone Oral Suspension
Reason of the recall: Microbial contamination
FDA Recall date: August 04, 2022

In case you experienced harm from any of these products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Source: fda.gov
See Less
458


Vi-Jon, LLC is revising a previously reported list of all flavors of Magnesium Citrate Saline Laxative Oral Solution within expiry that were voluntarily recalled to the consumer level to include product that was distributed in the United States, Canada and Panama. This includes all lots of Cherry... See More Flavor and Grape Flavor of Magnesium Citrate Saline Laxative Oral Solution, 10 FL OZ (296 mL) within expiry. To date, Vi-Jon, LLC is aware of 3 (three) reports of serious adverse reactions potentially related to this recall. Vi-Jon, LLC is in the process of investigating these reports.

On July 14, 2022, Vi-Jon, LLC recalled all lots of Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor, 10 FL OZ (296 mL) within expiry. The recall was initiated after Vi-Jon, LLCs third party microbial testing identified the presence of Gluconacetobacter liquefaciens.

Risk Statement: Immunocompromised patients, who consume this product, may be at increased risk for invasive infections caused by Gluconacetobacter liquefaciens that could lead to serious, life-threatening adverse health consequences. The product is used for relief of occasional constipation (irregularity) and generally produces bowel movement in ½ to 6 hours. The product is packaged in a 10 oz clear round plastic bottle. In addition to the lemon flavor, the recall includes the Cherry flavor and Grape flavor.

On August 3, 2022, the Recall product list has been updated to include the products noted below.

CANADA Equate Canada 300 mL Lemon Magnesium Citrate
NPN # NPN 80015316
UPC # 079068004923

CANADA Life 300 mL Lemon Magnesium Citrat
NPN # NPN 80015316
UPC # 057800856412

CANADA Life 300 mL Cherry Magnesium Citrate
NPN # NPN 80015316
UPC # 057800856405

CANADA Personnelle 300 mL Lemon Citrate
NPN # NPN 80015316
UPC # 055989029306

PANAMA CRUZ BLANC 10OZ LEMON MAG CIT
NPN # N/A
UPC # 308697403082

The product was distributed in the United States, Canada and Panama to wholesale and retail outlets. Vi-Jon, LLC is continuing their investigation into the cause of the problem.

Vi-Jon, LLC is notifying its customers by phone and email and is arranging for return or destruction of all recalled product. Consumers that have this recalled product should stop using and return any remaining product to the place of purchase.

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

In case you experienced harm from these products, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Vi-Jon, LLC
Brand name: Multiple brand names
Product recalled: Magnesium Citrate Saline Laxative Oral Solution
Reason of the recall: Microbial contamination with Gluconacetobacter liquefaciens
FDA Recall date: August 04, 2022

Source: fda.gov
See Less
458


The FDA is cautioning pet owners not to feed their pets certain lots of Darwin’s Natural Pet Products raw cat food after samples from these lots tested positive for Salmonella, and they represent a serious threat to human and animal health. These products are manufactured by Arrow... See More Reliance Inc., doing business as Darwin’s Natural Pet Products, and are sold online direct to consumers. These foods have been associated with cases of illness in three kittens in a single household.

The FDA recommended that Arrow Reliance Inc. voluntarily recall these products and notify the public, but the company has not done so.

The affected products are:
- Darwin’s Natural Pet Products Natural Selections Antibiotic & Grain Free Chicken Recipe for Cats, Lot 9116, manufactured on May 2, 2022.
- Darwin’s Natural Pet Products Natural Selections Antibiotic & Grain Free Turkey Recipe for Cats, Lot 9121, manufactured on May 4, 2022.

The products are sold in white and clear plastic packages with blue and green labeling. Each pack weighs two pounds and consists of four separate units. The lot codes are on the front lower left unit of the package.

If you have these lots of Darwin’s Natural Pet Food, or you can’t be sure of the lot code of the products you have, throw them away. Do not feed them to your pets.

Pet foods contaminated with Salmonella are of particular public health importance because they can affect both human and animal health. Pets can get sick from Salmonella and may also be carriers of the bacteria and pass it on to their human companions without appearing to be ill. People who think their pets have become ill after consuming contaminated pet food should first contact their veterinarians.

In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Source: fda.gov
See Less
458


The CFIA announced the recall of raw frozen Primal Patties for Dogs Beef Formula because it may be contaminated with Listeria monocytogenes, posing a risk of cross-contamination and illness after handling the pet food. This product was sold in British Columbia. As of August 2, 2022, the... See More company has not received any reports of incidents or illness in Canada.

The recalled product is:
- Primal Patties – Beef Formula, 6 lb, Case UPC: 854495006173, Unit UPC: 850334004164, Lot code number: W10068709, Best by date: 05/22/23.

The lot code number and best by date can be found on the back of the product packaging above the Primal Pet Foods Inc. red oval logo. Only lot code number W10068709 is included is this recall.

Animals that become infected with Listeria monocytogenes could display symptoms similar to humans. Listeria monocytogenes can affect animals eating the product, and there is risk to humans from handling the products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to the products.

Consumers should immediately stop using the recalled product and dispose of the product.

In case you are experiencing Listeria monocytogenes symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain, and diarrhea, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care. If symptoms persist, seek medical care.

Source: recalls-rappels.canada.ca
See Less
14


Grant County PSD has LIFTED the boil water advisory for the Huffman Drive, Rough Run, Spring Run, Boot Hill, Creite Village, Turkey Knob, and Tom Cox Road areas.

Source: twitter.com
Published: 2022-08-11 See Less
23


Today the Shippensburg Borough Authority had a water main break and is implementing precautionary boil water advisory. Affected customers include:
Eberly Drive
Logan Lane
Baker & Russell Drive
Volvo Way
Rowe Road

Source: twitter.com
Published: 2022-08-11 See Less
171


Recent Interesting Reports

Smyrna, TN, Vi-Jon, LLC is expanding its voluntary recall to include all lots of Magnesium Citrate Saline Laxative Oral Solution Lemon Flavor, 10 FL OZ (296 mL) within expiry to the consumer level. The product was distributed Nationwide to wholesale and retail outlets. To date, Vi-Jon, LLC... See More has received one report of an adverse reaction potentially related to this recall.

The recall was initiated after 3rd Party and Vi-Jon, LLC microbial testing identified the presence of Gluconacetobacter liquefaciens.

Risk Statement: Immunocompromised patients, who consume this product, may be at increased risk for invasive infections caused by Gluconacetobacter liquefaciens that could lead to serious, life-threatening adverse health consequences.

Vi-Jon, LLC is in the process of investigating this report. The product is used for relief of occasional constipation (irregularity) and generally produces bowel movement in ½ to 6 hours. The product is packaged in a 10 oz clear round plastic bottle.

The affected brands of Magnesium Citrate Laxative Oral Solution Lemon Flavor manufactured at Vi-Jon, LLC in Smyrna, TN are:

- Affected Brand: BEST CHOICE 10OZ LEMON MAG CIT. NDC # 63941-533-38. UPC # 70038200499.
- Affected Brand: CARE ONE 10OZ LEMON MAG CIT. NDC # 72476-001-38. UPC # 341520313226.
- Affected Brand: CARIBA 10OZ LEMON MAG CITRATE. NDC # 67860-166-38. UPC # 646702057012.
- Affected Brand: CRUZ BLANC 10OZ LEMON MAG CIT. NDC # N/A. UPC # 308697403082.
- Affected Brand: CVS 10OZ LEMON MAG CIT. NDC # 63868-929-38. UPC # 50428335178.
- Affected Brand: CVS 10OZ LEMON MAG CIT. NDC # 69842-983-38. UPC # 50428305942.
- Affected Brand: DISCOUNT DRUG MART 10OZ LEMON MAG CITRATE. NDC # 53943-166-38. UPC # 93351028205.
- Affected Brand: EQUALINE 10OZ LEMON MAG CIT. NDC # 41163-709-38. UPC # 41163500679.
- Affected Brand: EQUATE 10OZ LEMON MAG CIT SRP. NDC # 49035-506-38. UPC # 681131287142.
- Affected Brand: EXCHANGE SELECT 10OZ LEMON MAG CIT. NDC # 55301-166-38. UPC # 614299404205.
- Affected Brand: FAMILY WELLNESS 10OZ LEMON CITRATE. NDC # 55319-666-38. UPC # 32251580826.
- Affected Brand: GOOD SENSE 10OZ LEMON MAG CIT. NDC # 50804-166-38. UPC # 846036007374.
- Affected Brand: HARRIS TEETER 10OZ LEMON MAG CITRATE. NDC # 72036-002-38. UPC # 72036726124.
- Affected Brand: HEB 10OZ LEMON MAG CITRATE. NDC # 37808-769-38. UPC # 41220510863.
- Affected Brand: HEALTH MART 10OZ LEMON MAG CIT. NDC # 62011-0380-1. UPC # 52569142158.
- Affected Brand: KROGER 10OZ LEMON MAG CITRATE. NDC # 30142-899-38. UPC # 41260001826.
- Affected Brand: LEADER 10OZ LEMON MAG CIT. NDC # 70000-0424-1. UPC # 96295135541.
- Affected Brand: MAJOR 10OZ LEMON MAG CITRATE. NDC # 0904-6787-44. UPC # 309046787440.
- Affected Brand: MEIJER 10OZ LEMON MAG CIT. NDC # 41250-708-38. UPC # 713733459457.
- Affected Brand: PREMIER VALUE 10OZ LOW SOD LEM CIT. NDC # 68016-696-38. UPC # 840986035302.
- Affected Brand: PUBLIX 10OZ LEMON MAG CIT. NDC # 56062-266-38. UPC # 41415506732.
- Affected Brand: QUALITY CHOICE 10OZ LEMON MAG CIT. NDC # 63868-929-38. UPC # 635515901254.
- Affected Brand: REXALL 10OZ LEMON MAG CITRATE. NDC # 55910-183-38. UPC # 72785134188.
- Affected Brand: RITE AID 10OZ LEMON CITRATE. NDC # 11822-4330-2. UPC # 11822433006.
- Affected Brand: SIGNATURE CARE 10OZ LEMON MAG CIT. NDC # 21130-709-38. UPC # 321130779155.
- Affected Brand: SOUND BODY 10OZ LEMON MAG CIT. NDC # 50594-166-38. UPC # 72785114791.
- Affected Brand: SUNMARK 10OZ LEMON MAG CIT. NDC # 70677-0051-1. UPC # 10939908445.
- Affected Brand: SWAN 10OZ LEMON MAG CITRATE. NDC # 0869-0166-38. UPC # 72785134058.
- Affected Brand: TOPCARE 10OZ LEMON MAG CITRATE. NDC # 36800-709-38. UPC # 36800455290.
- Affected Brand: UP&UP 10OZ LEMON MAG CIT. NDC # 11673-708-38. UPC # 72785128835.
- Affected Brand: UP&UP 10OZ LEMON MAG CIT. NDC # 11673-666-38. UPC # 72785128835.
- Affected Brand: WALGREENS 10OZ LEMON MAG CIT. NDC # 0363-8166-38. UPC # 311917201603.

Vi-Jon, LLC is continuing their investigation into the cause of the problem. This recall is being conducted with the knowledge of the U.S. Food and Drug Administration.

Company name: Vi-Jon, LLC
Brand name: Multiple brand names
Product recalled: Magnesium Citrate Saline Laxative Oral Solution, Lemon Flavor
Reason of the recall: Microbial contamination with Gluconacetobacter liquefaciens
FDA Recall date: July 15, 2022

Source: fda.gov
See Less
458


Well we got the treats and my dogs had diarrhea and vomiting and they won’t stop | Symptoms: Diarrhea, Vomiting See Less
Dream Bone dog treats photo #1 Dream Bone dog treats photo #1
nsfw
Dream Bone dog treats photo #2
nsfw
133


Edgewell Personal Care Company (NYSE: EPC) today issued a voluntary nationwide recall of three batches of Banana Boat Hair & Scalp Sunscreen Spray SPF 30 to the consumer level as outlined in the list below. An internal review found that some samples of the product contained trace... See More levels of benzene. While benzene is not an ingredient in any Banana Boat products, the review showed that unexpected levels of benzene came from the propellant that sprays the product out of the can. To date, Edgewell has not received any adverse events related to this recall. The products were distributed nationwide in the United States through various retailers and online. Edgewell has notified its retailers to remove any remaining recalled product from shelves.

Benzene is classified as a human carcinogen. Exposure to benzene can occur by inhalation, orally, and through the skin and it potentially can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life threatening. Benzene is ubiquitous in the environment. Humans around the world have daily exposures to it indoors and outdoors from multiple sources. Daily exposure to benzene in the recalled products would not be expected to cause adverse health consequences according to an independent health assessment using established exposure modeling guidelines.

Importantly, no other batches of Hair & Scalp (either before or after these batch codes) and no other Banana Boat products are in the scope of this recall and may continue to be used by consumers safely and as intended.

UPC: 0-79656-04041-8, DESCRIPTION: Banana Boat Hair & Scalp Spray SPF 30, Lot Code: 20016AF, Expiration: December 2022, Size: 6 oz
UPC: 0-79656-04041-8, DESCRIPTION: Banana Boat Hair & Scalp Spray SPF 30, Lot Code: 20084BF, Expiration: February 2023, Size: 6 oz
UPC: 0-79656-04041-8, DESCRIPTION: Banana Boat Hair & Scalp Spray SPF 30, Lot Code: 21139AF, Expiration: April 2024, Size: 6 oz

The voluntarily recalled sunscreen spray products are packaged in aerosol cans. Banana Boat will also offer reimbursement for consumers who have purchased a product marked with one of the lot codes in the table above. Lot codes are located on the bottom of the can. Consumers should stop using the affected product immediately and appropriately discard.

In case you experienced harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Edgewell Personal Care Company
Brand name: Banana Boat
Product recalled: Hair & scalp sunscreen spray
Reason of the recall: Due to presence of benzene
FDA Recall date: July 29, 2022

Source: fda.gov
See Less
459


The FDA is cautioning pet owners not to feed their pets certain lots of Darwin’s Natural Pet Products raw cat food after samples from these lots tested positive for Salmonella, and they represent a serious threat to human and animal health. These products are manufactured by Arrow... See More Reliance Inc., doing business as Darwin’s Natural Pet Products, and are sold online direct to consumers. These foods have been associated with cases of illness in three kittens in a single household.

The FDA recommended that Arrow Reliance Inc. voluntarily recall these products and notify the public, but the company has not done so.

The affected products are:
- Darwin’s Natural Pet Products Natural Selections Antibiotic & Grain Free Chicken Recipe for Cats, Lot 9116, manufactured on May 2, 2022.
- Darwin’s Natural Pet Products Natural Selections Antibiotic & Grain Free Turkey Recipe for Cats, Lot 9121, manufactured on May 4, 2022.

The products are sold in white and clear plastic packages with blue and green labeling. Each pack weighs two pounds and consists of four separate units. The lot codes are on the front lower left unit of the package.

If you have these lots of Darwin’s Natural Pet Food, or you can’t be sure of the lot code of the products you have, throw them away. Do not feed them to your pets.

Pet foods contaminated with Salmonella are of particular public health importance because they can affect both human and animal health. Pets can get sick from Salmonella and may also be carriers of the bacteria and pass it on to their human companions without appearing to be ill. People who think their pets have become ill after consuming contaminated pet food should first contact their veterinarians.

In case you are experiencing Salmonella symptoms such as diarrhea, abdominal cramps, and fever, it is important to report it. It can help to detect & resolve outbreaks early and prevent others from being harmed, and it enables better surveillance. If symptoms persist, seek medical care.

Source: fda.gov
See Less
458


I am a resident of 817 Rose Lane and over a period of nearly 4 weeks I’ve reported a dead branch on a tree on the parkway hanging over my driveway and street. It nearly scrapes the top of my car and my lawncare people have to... See More duck the branch to cut my grass. This is dangerous and I have had no active response from public works. Spoke to someone from public works and city hall with no results 3 times. See Less
4.8K


This product was found to contain the undeclared active pharmaceutical ingredient tadalafil. Tadalafil, which is a phosphodiesterase type-5 (PDE-5) inhibitor, is the active ingredient in an FDA-approved prescription drug, used to treat erectile dysfunction (ED). Product was sold through our website, wholesaleonline1.com Mar 2022 to July 2022... See More and ­ distributed in any US State. To date, wholesaleonline1.comhas not received any reports of adverse events related to this recall.

The product comes in a black box and contains 12 sachets of 15 grams of honey with different expiration dates stamped on the back side. This undeclared ingredient (tadalafil) may interact with nitrates found in some prescription drugs such as nitroglycerin and may lower blood pressure to dangerous levels. Men with diabetes, high blood pressure, high cholesterol, or heart disease often take nitrates.

The recall was initiated after FDA laboratory analysis confirmed that Dose Vital VIP Vital Honey contains the undeclared active pharmaceutical ingredient Tadalafil. Consumers who have purchased Vital Honey on wholesaleonline1.com are urged to immediately discontinue use and return the recalled product for a full refund.

In case you experienced harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: MKS Enterprise LLC
Brand name: Dose Vital
Product recalled: Honey
Reason of the recall: Undeclared active pharmaceutical ingredient tadalafil
FDA Recall date: July 19, 2022

Source: fda.gov
See Less
458


Dream bones killed my 11 yr old dog yesterday! Rubie was my life & loved her so much. I gave these bones to her because she loved them & they caused a blockage & perforated her bowel which she became septic & died within 2days. I plan... See More on destroying every dream bones bag I see in the stores until they stop selling them. I can only hope by doin this it might save atleast one dogs life. SAVE A DOG & DESTROY THESE BONES!! See Less
1.1K


Encore is recalling Beef Selection in Gravy multipack dog food because the Beef Steak with Potatoes in Gravy tin, within the multipack, may contain small pieces of metal. This product was distributed nationwide in the United Kingdom.

Encore Beef Selection in Gravy (Multipack) (5 tins x 156g)... See More Batch code: LU1-343
Best before: 09 December 2024

Encore Beef Selection in Gravy (Multipack) (5 tins x 156g)
Batch code: LU1-302
Best before: 29 October 2024

Encore Beef Steak with Potatoes in Gravy (Individual tin) (156g)
Batch code: LU1343D
Best before: December 2024

Pet-owners: We urge customers who have bought this product not to feed it to their dog and return it to the store with or without a receipt from where it was bought for a full refund.

In case your pet experienced harm from extraneous materials, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Encore
Product recalled: Encore Beef Selection in Gravy (Multipack), Encore Beef Selection in Gravy (Multipack), Encore Beef Steak with Potatoes in Gravy (Individual tin)
FSA Recall date: 07/18/2022

Source: food.gov.uk
See Less
52


Ultra Supplement LLC is voluntarily recalling lot number DAP272109, exp 4/1/26 of Sustango capsules packaged in 10-count blisters packaged in a carton to the consumer level. Ultra Supplement was notified by Amazon that laboratory analysis has found the product to be tainted with tadalafil, an ingredient in... See More FDA approved products for treatment of male erectile dysfunction in the family of drugs known as phosphodiesterase (PDE-5) inhibitors. The product was distributed via the internet and fulfilled by Amazon at www.amazon.com nationwide in the USA. To date, Ultra Supplement has not received any reports of adverse events related to this recall.

On December 17, 2020, FDA issued a press release that warned consumers to avoid certain products found on Amazon, eBay and other retailers due to hidden and potentially dangerous drug ingredients. It also encouraged online marketplaces to ensure these products are not sold on their platforms.

The presence of tadalafil in Sustango makes this product an unapproved drug for which the safety and efficacy has not been established and therefore, subject to recall.

Consumers with underlying medical issues who take Sustango capsules with undeclared tadalafil may experience health risks. For example, PDE-5 inhibitors may interact with nitrates found in some prescription drugs (such as nitroglycerin) lowering blood pressure to dangerous levels that may be life-threatening. Consumers with diabetes, high blood pressure, or heart disease often take nitrates. The product is marketed as a dietary supplement for male enhancement and is packaged in 10-count blisters packaged in a carton, ASIN X0024468I9. The affected cartons include Lot DAP272109, Exp. 4/1/26. The product can be identified by the label below.

Ultra Supplement is notifying its distributors and customers by this press announcement and by Amazon Messaging and is arranging for return of all recalled products. Consumers that have Sustango capsules Lot# DAP272109 should stop using the product.

In case you experienced harm from this product, it is important to report it. It can help to detect & resolve issues and prevent others from being harmed, and it enables better surveillance.

Company name: Ultra Supplement LLC
Brand name: Sustango
Product recalled: Dietary Supplement for Male Enhancement
Reason of the recall: Undeclared Tadalafil
FDA Recall date: July 25, 2022

Source: fda.gov
See Less
458


Last 30 days