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Medically Minded Hand Sanitizer - recalled due to presence of methanol, USA

May 13, 2021 2:01 PM

United States

Company name: Global Sanitizers
Brand name: Medically Minded
Product recalled: Hand Sanitizer
Reason of the recall: Presence of methanol
FDA Recall date: May 13, 2021
Recall details: Las Vegas, NV, Global Sanitizers is voluntarily recalling 50 thousand units of Medically Minded hand sanitizers, lot numbers: E212020 & E082020 Best Buy of 5/21/2022 to the user/consumer level. FDA analysis has found the product to contain methanol.

Risk Statement: Substantial methanol exposure can result in coma, seizures, permanent blindness, permanent damage to the central nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidently ingest these products and adolescents and adults who drink these products as an alcohol (ethanol) substitute, are most at risk for methanol poisoning.

To date, Global Sanitizers has not received any reports of adverse events related to this recall. These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available. Medically Minded hand sanitizer is packaged in 8.5 oz / 250 ml clear bottles with caps with the following UPC 7675300359. The affected Medically Minded hand sanitizer lots include the following lot numbers and expiration dates E212020 & E082020 Best Buy of 5/21/2022. The product can be identified by the representative label below.

The hand sanitizer was distributed Nationwide in the USA to Wholesale companies who further distributed between July 2020 -August 2020. Global Sanitizers is notifying its distributors and customers by Email, Letter, Telephone & Press Release and is arranging for return of all recalled products. Consumers/distributors/retailers that have Medically Minded hand sanitizer product which is being recalled should stop using/return to place of purchase/discard/contact their doctor.

Consumers with questions regarding this recall can contact Global Sanitizers by calling 702.323.4402 or e-mail address recall@globalsanitizers.com Monday through Friday 9am-5pm pacific standard time. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this drug product.

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

Check the full recall details on fda.gov

Source: FDA

More incidents from:
Drugs
Recall
United States

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June 8, 2021 10:00 PM

“Company name: Hubbard Feeds
Brand name: Hubbard Feeds
Product recalled: EASY FEED ORGANIC CHICK STARTER/GROWER ORG
Reason of the recall: Contains deficient levels of salt
FDA Recall date: June 08, 2021
Recall details: Hubbard Feeds is voluntarily recalling EASY FEED ORGANIC CHICK STARTER/GROWER... See MoreORG with batch number B01785781. The product has been found to contain deficient levels of salt. Low sodium may cause abnormal nerve impulses so chicks’ muscles will not move well. Low sodium can also affect the cell’s normal internal pressure which can affect cardiac output due to deflated muscle not working well. The growth of birds may also be negatively impacted.

This recall relates only to EASY FEED ORGANIC CHICK STARTER/GROWER ORG distributed in the state of Colorado, with the following batch number printed on the package:

- Product Name: Easy Feed Organic Chick Starter/Grower Org
- Batch/Lot#: B01785781
- Item No./Product No.: 53266
- Package Info.:40# Bag

Check the full recall details on fda.gov

Source: FDA
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June 11, 2021 9:02 PM

“Company name: Viona Pharmaceuticals Inc.
Brand name: Viona Pharmaceuticals Inc.
Product recalled: Metformin Hydrochloride Extended-Release Tablets
Reason of the recall: Contains Nitrosodimethylamine (NDMA) impurities
FDA Recall date: June 11, 2021
Recall details: Viona Pharmaceuticals Inc., is... See Morevoluntarily recalling 2 (two) lots of Metformin Hydrochloride Extended-Release Tablets, USP 750 mg to the retail level. The 2 (two) lots of Metformin Hydrochloride Extended-Release Tablets, USP 750 mg have been found to contain levels of Nitrosodimethylamine (NDMA) impurities above acceptable daily limits. This product was manufactured by Cadila Healthcare Limited, Ahmedabad, India in November 2019, for U.S. distribution by Viona Pharmaceuticals Inc.

Risk Statement: NDMA is classified as a probable human carcinogen (a substance that could cause cancer) based on results from laboratory tests. NDMA is a known environmental contaminant and found in water and foods, including meats, dairy products, and vegetables. Patients who have received impacted lots of Metformin Hydrochloride Extended-Release Tablets, USP 750 mg are advised to continue taking their medication and contact their physician for advice regarding an alternative treatment.

According to the FDA, it could be dangerous for patients with this serious condition to stop taking their Metformin without first talking to their healthcare professionals. Please visit the agency’s website for more information at fda.gov To date, neither Viona Pharmaceuticals Inc., nor Cadila Healthcare Limited have received any reports of adverse events related to this recall.

The product is used as an adjunct to diet and exercise to improve blood glucose control in adults with type 2 diabetes mellitus and is packaged in HDPE bottles of 100 tablets, under NDC 72578-036-01. The affected Metformin Hydrochloride Extended-Release Tablets, USP 750 mg are listed in the below table. The product can be identified as white to off-white, capsule shaped, uncoated tablets, debossed with "Z", "C" on one side and "20" on the other side. Metformin Hydrochloride Extended-Release Tablets, USP 750 mg was distributed Nationwide to Distributors.

- Metformin Hydrochloride Extended-Release Tablets, USP 750 mg. NDC No: 72578-036-01. Batch No: M915601. Exp. Date: Oct-2021.

Check the full recall details on fda.gov

Source: FDA
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June 11, 2021 10:00 PM

“Company name: Purina Animal Nutrition
Brand name: Purina
Product recalled: Beef Cattle Feed RangeLand® 30-13 TUB
Reason of the recall: Tubs that are too soft, allowing over-consumption which can lead to urea toxicity.
FDA Recall date: June 11, 2021
Recall details: Purina Animal Nutrition is ini... See Moretiating a very limited voluntary recall of one lot of Purina® RangeLand® 30-13 (125#) beef cattle feed. This recall is being initiated as a precaution related to tubs that are too soft, allowing over-consumption, which could result in urea toxicity.

Purina Animal Nutrition received reports from customers claiming the feed may have resulted in poor health and/or death. Elevated urea levels can cause health issues and potential death in cattle. Symptoms of excess urea may include muscle tremors (especially of the face and ears), abdominal pain, frothy salivation, polyuria, and bruxism (grinding of teeth). The affected product and lot number is:

- Formula No: L3B3. Item No: 1800049-627. Description: Purina® RangeLand® 30-13 (125#). Lot Number: 1MAR19CLF1

The affected feed was manufactured by Purina Animal Nutrition on March 19, 2021. The affected Purina® feed was sold in the following states: Arizona, Arkansas, Hawaii, Idaho, Louisiana, Mississippi, New Mexico, Oklahoma, Oregon, Texas, Washington.

Customers can find the lot number on the side of each tub. Customers who purchased this product are instructed to stop feeding and to destroy or return it to the point of purchase.

Check the full recall details on fda.gov

Source: FDA
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June 13, 2021 1:00 PM

“Company name: Freshpet Inc.
Brand name: Freshpet
Product recalled: Select Small Dog Bite Size Beef & Egg Recipe Dog Food
Reason of the recall: Potential for Salmonella
FDA Recall date: June 13, 2021
Recall details: Freshpet Inc. is announcing a voluntary recall of a single lot of Freshpet® Se... See Morelect Small Dog Bite Size Beef & Egg Recipe Dog Food (1 LB bags), with Sell by Date 10/30/2021,due to potential contamination with Salmonella. Our Freshpet Team had designated this single lot for destruction, but it was inadvertently shipped to retailers in limited geographic markets between June 7 to June 10, 2021. No other Freshpet products or lot codes are impacted by this recall.

Salmonella can affect animals eating the product and there is risk to humans from handling contaminated products, especially if they have not thoroughly washed their hands after having contact with the products or any surfaces exposed to these products. Healthy people infected with Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms. Consumers exhibiting these signs after having contact with this product should contact their healthcare providers.

Dogs with Salmonella infections may be lethargic and have diarrhea or bloody diarrhea, fever, and vomiting. Some dogs will have only decreased appetite, fever and abdominal pain. Infected but otherwise healthy dogs can be carriers and infect other animals or humans. If your dog has consumed the recalled product and has these symptoms, please contact your veterinarian.

Freshpet has received no reports of illness, injury, or adverse reaction to date, and has issued this recall because of our deep commitment to the safety of our pet parents and their dogs. The limited number of impacted products may have been sold at: Publix in Florida, South Carolina, and Georgia, and at limited Target locations in Arizona and Southern California.

Most of the product was intercepted at retailer distribution warehouses and not delivered to retail stores. If pet parents have products matching the following description in their possession, they should stop feeding it to their dogs and dispose of it immediately.  

Please see the product pictures and the information below for details.

- Product Name: FRESHPET® SELECT SMALL DOG BITE SIZE BEEF & EGG RECIPE
- Retail UPC Code: 627975012939
- Lot Code: 1421FBP0101
- Sell-by Date: 10/30/2021 L2

Check the full recall details on fda.gov

Source: FDA
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June 15, 2021 8:00 PM

“Company name: Fold Hill Foods
Brand name: Fold Hill Food
Product recalled: Applaws Cat Dry Chicken, Applaws Cat Dry Chicken & Salmon, AVA Adult Fish, AVA Adult Mature Chicken 7+, AVA Senior Chicken 12+, AVA Sensitive Skin & Stomach, AVA Weight Management, AVA Hairball, AVA Oral Care, AVA British S... See Morehorthair, AVA Persian, AVA Maine Coon, Applaws Kitten Dry Chicken, by Sainsbury’s Hypoallergenic Recipe complete dry cat food with Salmon 1+ Years, by Sainsbury’s Hypoallergenic Recipe complete dry cat food with Chicken 1+ Years, Applaws Cat Dry Chicken & Lamb, Applaws Cat Dry Chicken & Duck, Applaws Cat Dry Ocean Fish, Applaws Cat Dry Senior Chicken, Product, AVA Kitten Chicken, AVA Adult Chicken
FSA Recall date: 06/15/2021
Recall details: Fold Hill Foods is taking the precautionary action of recalling several hypoallergenic cat food products because of safety concerns.

- Applaws Cat Dry Chicken (400g, 2kg and 7.5kg)
- Applaws Cat Dry Chicken & Salmon (400g, 2kg and 7.5kg)
- AVA Adult Fish (2kg)
- AVA Adult Mature Chicken 7+ (2kg and 4kg)
- AVA Senior Chicken 12+ (2kg)
- AVA Sensitive Skin & Stomach (1.5kg)
- AVA Weight Management (1.5kg)
- AVA Hairball (1.5kg)
- AVA Oral Care (1.5kg)
- AVA British Shorthair (1.5kg)
- AVA Persian (1.5kg)
- AVA Maine Coon (1.5kg)
- Applaws Kitten Dry Chicken (400g, 2kg and 7.5kg)
- by Sainsbury’s Hypoallergenic Recipe complete dry cat food with Salmon 1+ Years (800g)
- by Sainsbury’s Hypoallergenic Recipe complete dry cat food with Chicken 1+ Years (800g)
- Applaws Cat Dry Chicken & Lamb (400g, 2kg and 7.5kg)
- Applaws Cat Dry Chicken & Duck (400g, 2kg and 7.5kg)
- Applaws Cat Dry Ocean Fish (350g, 1.8kg and 6kg)
- Applaws Cat Dry Senior Chicken (400g, 2kg and 7.5kg)
- AVA Kitten Chicken (300g and 2kg)
- AVA Adult Chicken (300g, 2kg and 4kg)

Check the full detailed list of the recalled products in the link below.

If you have bought any of the above products you should stop feeding them to your cat. If cat owners are concerned about the health of their pet then they should seek immediate advice from their vet.

There has been an increase in cases of pancytopenia in cats and there is a possible link to the cat food products listed above. Pancytopenia is a very rare condition wherein the number of blood cells (red, white, and platelets) rapidly decreases, causing serious illness.

Check the full recall details on food.gov.uk

Source: FSA
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June 15, 2021 7:00 PM

“Company name: Philips
Brand name: Philips
Product recalled: Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices
Reason of the recall: Potential health risks related to the polyester-based polyurethane (PE-PUR) so... See Moreund abatement foam component in these devices
FDA Recall date: June 15, 2021
Recall details:
- Philips is initiating a voluntary recall notification* to ensure patient safety in consultation with regulatory agencies
- Corrective actions include the deployment of updated instructions for use and a repair and replacement program for affected devices
- Philips aims to address all affected devices within the scope of this correction as expeditiously as possible.

Amsterdam, the Netherlands – Following the company update on April 26, 2021, Royal Philips(NYSE: PHG; AEX: PHIA) today provides an update on the recall notification* for specific Philips Bi-Level Positive Airway Pressure (Bi-Level PAP), Continuous Positive Airway Pressure (CPAP), and mechanical ventilator devices to address identified potential health risks related to the polyester-based polyurethane (PE-PUR) sound abatement foam component in these devices. The majority of the affected devices within the advised 5-year service life are in the first-generation DreamStation product family.

To date, Philips has produced millions of Bi-Level PAP, CPAP and mechanical ventilator devices using the PE-PUR sound abatement foam. Despite a low complaint rate (0.03% in 2020), Philips determined based on testing that there are possible risks to users related to this type of foam. The risks include that the PE-PUR foam may degrade into particles which may enter the device’s air pathway and be ingested or inhaled by the user, and the foam may off-gas certain chemicals. The foam degradation may be exacerbated by use of unapproved cleaning methods, such as ozone,** and high heat and high humidity environments may also contribute to foam degradation.

Therefore, Philips has decided to voluntarily issue a recall notification* to inform patients and customers of potential impacts on patient health and clinical use related to this issue, as well as instructions on actions to be taken.

Recall notification* advise for patients and customers. Based on the latest analysis of potential health risks and out of an abundance of caution, the recall notification* advises patients and customers to take the following actions:

- For patients using affected BiLevel PAP and CPAP devices: Discontinue use of your device and work with your physician or Durable Medical Equipment (DME) provider to determine the most appropriate options for continued treatment. To continue use of your device due to lack of alternatives, consult with your physician to determine if the benefit of continuing therapy with your device outweighs the risks identified in the recall notification.*

- For patients using affected life-sustaining mechanical ventilator devices: Do not stop or alter your prescribed therapy until you have talked to your physician. Philips recognizes that alternate ventilator options for therapy may not exist or may be severely limited for patients who require a ventilator for life-sustaining therapy, or in cases where therapy disruption is unacceptable. In these situations, and at the discretion of the treating clinical team, the benefit of continued usage of these ventilator devices may outweigh the risks identified in the recall notification.*

Possible health risks: The company continues to monitor reports of potential safety issues as required by medical device regulations and laws in the markets in which it operates. To date, there have been no reports of death as a result of these issues.

Philips has received reports of possible patient impact due to foam degradation. The potential risks of particulate exposure include headache, irritation, inflammation, respiratory issues, and possible toxic and carcinogenic effects.

The potential risks of chemical exposure due to off-gassing include headache, irritation, hypersensitivity, nausea/vomiting, and possible toxic and carcinogenic effects. Philips has received no reports regarding patient impact related to chemical emissions.

*This is a recall notification for the US only, and a field safety notice for the rest of the world
**Potential Risks Associated With The Use of Ozone and Ultraviolet (UV) Light Products for Cleaning CPAP Machines and Accessories: FDA Safety Communication.

Check the full recall details on fda.gov

Source: FDA
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June 16, 2021 8:00 PM

“Company name: Fold Hill Foods
Product recalled: Applaws Cat Dry Chicken, Applaws Cat Dry Chicken & Salmon, AVA Adult Mature Chicken 7+, AVA Senior Chicken 12+, AVA Sensitive Skin & Stomach, AVA Weight Management, AVA Hairball, AVA Oral Care, AVA British Shorthair, AVA Persian, AVA Maine Coon, by Sa... See Moreinsbury’s Hypoallergenic Recipe complete dry cat food with Salmon 1+ Years, Applaws Kitten Dry Chicken, by Sainsbury’s Hypoallergenic Recipe complete dry cat food with Chicken 1+ Years, Applaws Cat Dry Chicken & Lamb, Applaws Cat Dry Chicken & Duck, Applaws Cat Dry Ocean Fish, Applaws Cat Dry Senior Chicken, AVA Kitten Chicken, AVA Adult Chicken, AVA Adult Fish
FSA Recall date: 06/16/2021
Recall details: Fold Hill Foods is taking the precautionary action of recalling several hypoallergenic cat food products because of safety concerns. This product recall information notice has been updated to include all best before dates for Applaws products with the site code GB218E5009. This is not due to the identification of further safety concerns, but is a voluntary action by the manufacturer to make things easier for consumers to understand which products have been affected.

- Applaws Cat Dry Chicken (400g, 2kg and 7.5kg)
- Applaws Cat Dry Chicken & Salmon (400g, 2kg and 7.5kg)
- AVA Adult Mature Chicken 7+ (2kg and 4kg)
- AVA Senior Chicken 12+ (2kg)
- AVA Sensitive Skin & Stomach (1.5kg)
- AVA Weight Management (1.5kg)
- AVA Hairball (1.5kg)
- AVA Oral Care (1.5kg)
- AVA British Shorthair (1.5kg)
- AVA Persian (1.5kg)
- AVA Maine Coon (1.5kg)
- by Sainsbury’s Hypoallergenic Recipe complete dry cat food with Salmon 1+ Years (800g)
- Applaws Kitten Dry Chicken (400g, 2kg and 7.5kg)
- by Sainsbury’s Hypoallergenic Recipe complete dry cat food with Chicken 1+ Years (800g)
- Applaws Cat Dry Chicken & Lamb (400g, 2kg and 7.5kg)
- Applaws Cat Dry Chicken & Duck (400g, 2kg and 7.5kg)
- Applaws Cat Dry Ocean Fish (350g, 1.8kg and 6kg)
- Applaws Cat Dry Senior Chicken (400g, 2kg and 7.5kg)
- AVA Kitten Chicken (300g and 2kg)
- AVA Adult Chicken (300g, 2kg and 4kg)
- AVA Adult Fish (2kg)

If you have bought any of the above products you should stop feeding them to your cat. If you have bought an AVA product contact www.petsathome.com and fill out the contact form on the help page or livechat. If you have bought an Applaws product contact www.applaws.com/uk/contact-us. If you have bought a Sainsbury’s product contact www.sainsburys.co.uk/help or their Customer Careline on 0800 636262. If cat owners are concerned about the health of their pet then they should seek immediate advice from their vet.

There is concern on the safety of the products listed above. There has been an increase in cases of pancytopenia in cats and there is a possible link to the cat food products listed above. Pancytopenia is a very rare condition wherein the number of blood cells (red, white, and platelets) rapidly decreases, causing serious illness.

Check the full recall details on food.gov.uk

Source: FSA
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2nd dose Pfizer vaccine, New York, NY, USA

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I started feeling chills after 12 hours then after 24 hours I got a mild fever, fatigue and arm pain till the day after. On the second day I had... See Morea headache for the entire day and that's it. On the third day after the vaccine I felt much better. It was worth it. See Less
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“Company name: Natural Balance Pet Foods, Inc.
Brand name: Natural Balance
Product recalled: L.I.D. Green Pea & Chicken Dry Cat Formula
Reason of the recall: Potential Salmonella Contamination
FDA Recall date: May 20, 2021
Recall details: Natural Balance Pet Foods, Inc. of San Diego, CA, is volu... See Morentarily recalling the cat food products listed below due to possible contamination with Salmonella. This was discovered from a routine state surveillance sample from the Minnesota Department of Agriculture.

Products were distributed nationwide in the U.S. via both retail and online distribution. No customer complaints or illnesses have been reported to date, and no other Natural Balance Pet Foods, Inc. products are impacted by this recall. Salmonella can infect cats eating a product contaminated with Salmonella bacteria.

Symptoms of Salmonella infection in cats may include vomiting, diarrhea, decreased appetite, fever, or excessive salivation. If your pet has consumed the recalled product and has these symptoms, please contact your veterinarian. Some cats may not appear sick but can spread infection to other animals and humans in the household.

Salmonella can spread to humans from handling contaminated pet products, especially if they have not washed their hands after having contact with their cat's foods, surfaces and/or cats that have been in contact with the contaminated product. Healthy people infected wit Salmonella should monitor themselves for some or all of the following symptoms: nausea, vomiting, diarrhea or bloody diarrhea, abdominal cramping and fever. Rarely, Salmonella can result in more serious ailments, including arterial infections, endocarditis, arthritis, muscle pain, eye irritation, and urinary tract symptoms.

People exhibiting these signs after having contact with this product or a cat that has eaten this product should contact their healthcare provider.

- 5 LB Bag, Natural Balance L.I.D. Limited Ingredient Diets Green Pea & Chicken Formula Dry Cat Food. Retail UPC: 2363300233. Lot Code: 1008080 06:42N811202:20. Best If Used by Date: 10-Mar-2022

- 10 LB Bag, Natural Balance L.I.D. Limited Ingredient Diets Green Pea & Chicken Formula Dry Cat Food. Retail UPC: 2363300235. Lot Code: 1008080 06:42N811202:20. Best If Used by Date: 10-Mar-2022

If pet parents have matching products in their possession, they should stop feeding it to their cats and dispose of it immediately or return it to their retailer for a refund. (See product photos below.) This information can be found on the back panel of each 5 LB and 10 LB bag. Natural Balance Pet Foods products are 100% guaranteed and all returned product will be refunded.

Check the full recall details on fda.gov

Source: FDA
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“Company name: Dibar Nutricional S. de R.L. de C.V.
Brand name: DIBAR Labs, ProtectoRx
Product recalled: Hand Sanitizer
Reason of the recall: Presence of methanol
FDA Recall date: May 19, 2021
Recall details: Morelia, Michoacán, Mexico, Dibar Nutricional S. de R.L. De C.V. (“Dibar”) is voluntari... See Morely recalling all Dibar Labs Hand Sanitizer packaged in 8oz and 16 oz bottles, respectively, to the consumer level (see Label 1 below). Dibar is also voluntarily recalling ProtectoRx Hand Sanitizer packaged in 2oz and 16oz fluid ounce bottles, respectively, to the consumer level (see Label 2 below), as well as all Advance Hand Sanitizer packaged in 16 oz bottles, likewise, to the consumer level (see Label 3 below). These products are being recalled after testing conducted by our firm revealed the presence of methanol.

Risk Statement: Substantial methanol exposure can result in nausea, vomiting, headache, blurred vision, permanent blindness, seizures, coma, permanent damage to the nervous system, or death. Although all persons using these products on their hands are at risk, young children who accidentally ingest the products and adolescents and adults who drink the products as an alcohol (ethanol) substitute are most at risk for methanol poisoning.

To date, the company has not received any reports of adverse reactions related to this recall. These products are used as hand sanitizers and marketed to help decrease bacteria on the skin when soap and water are not available.

The affected bottles of hand sanitizer include a twelvedigit lot code printed on the bottle near the base. The products can be identified by the label image provided at the end of this release. Products labeled as Dibar Labs Hand Sanitizer were distributed nationwide in the USA through S.E.N.D. LLC and its customers. Products labeled as ProtectoRx Hand Sanitizer were distributed in Puerto Rico through PR TRADING LLC and its customers. Products labeled as Advance Hand Sanitizer were distributed in the USA through RGV HEALTH SERVICES LLC DBA VALLEY and its customers.

Dibar Nutricional S. de R.L. De C.V., has notified its direct distributors by letter and asked that they remove the recalled products from commerce immediately if they still possess inventory.

Consumers, distributors and retailers that have the hand sanitizers which are being recalled should stop using, distributing and/or selling them and return them to the place of purchase. Consumers should contact their physician or healthcare provider if they have experienced any problems that may be related to taking or using this product. Adverse reactions or quality problems experienced with the use of this product may be reported to the FDA's MedWatch Adverse Event Reporting program either online by regular mail or by fax.

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

Check the full recall details on fda.gov

Source: FDA
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