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Meow Mix® Original Choice Dry Cat Food - recalled due to potential Salmonella, USA

April 12, 2021 1:00 PM

United States

Company name: J. M. Smucker Co.
Brand name: Meow Mix®
Product recalled: Meow Mix® Original Choice Dry Cat Food
Reason of the recall: Potential Salmonella Contamination
FDA Recall date: April 12, 2021
Recall details: Orrville, OH – The J. M. Smucker Co. today announced a limited, voluntary recall of two lots of Meow Mix® Original Choice Dry Cat Food (30LB bag) due to potential salmonella contamination. The Company has received no reports of pet illness or adverse reaction and has issued this recall out of an abundance of caution.

The impacted products were sold at select Walmart stores in IL, MO, NE, NM, OK, UT, WI, and WY. No other Meow Mix® products are impacted by this recall. If pet parents have products matching the following description in their possession, they should stop feeding it to their cats and dispose of it immediately. This information can be found on the bottom and back of each bag.

- Meow Mix® Original Choice Dry Cat Food (30 LB Bag). Retail UPC Code: 2927452099. Lot Code: 1081804. Best If Used By Date: 9/14/2022
- Meow Mix® Original Choice Dry Cat Food (30 LB Bag). Retail UPC Code: 2927452099. Lot Code: 1082804. Best If Used By Date: 9/15/2022

Check the full recall details on fda.gov

Source: FDA

Reported By SafelyHQ.com User

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May 10, 2021 4:00 PM

“Company name: Novo Nordisk
Brand name: Levemir, Tresiba, Fiasp, Novolog and Xultophy
Product recalled: Product Samples
Reason of the recall: Due to improper storage temperature conditions
FDA Recall date: May 10, 2021
Recall details: Novo Nordisk is voluntarily recalling 1,468 product samples... See Morelisted in the table below of Levemir®, Tresiba®, Fiasp®, Novolog® and Xultophy®, to the consumer level. These products are being recalled because they were stored at temperatures below storage requirements.

This recall only impacts product samples and does not impact product that has been broadly distributed to pharmacies or mail-order services. If product samples are exposed to temperatures below 32°F, it could cause a lack of efficacy and damage to the cartridge and pen-injectors. If product from an improperly stored vial, cartridge or pen-injector is used, there is a risk that you might not receive the right amount of medicine as intended which may lead to hyperglycemia or hypoglycemia resulting in adverse health consequences ranging from limited to life-threatening.

Novo Nordisk has not received any reports of serious adverse events or injuries related to this recall. These products are used to lower blood glucose levels in people with diabetes and are packaged in cartons with either a vial, pen-injector (FlexPen® or FlexTouch®) or a cartridge (PenFill®). A list of the affected lots can be found in the link below.

The product can be identified by looking for the batch number or lot number located on the product or carton and matching it to the list above. Novo Nordisk has notified all physician offices that received affected samples and requested all impacted samples be returned. Customers who received an affected sample through the physician’s office should have received a letter from their physician.

If product samples match a batch number or there are any questions about the recall, please contact the Novo Nordisk recall processor Inmar at 1-888-686-5002, Monday through Friday, 9:00 AM to 5:00 PM EDT. Please report any complaints and adverse events to Novo Nordisk's Customer Care Center which can be reached at 1-800-727-6500, Monday through Friday, 8:30 AM to 6:00 PM EDT.

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.

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

May 11, 2021 11:00 AM

“Company name: Yamtun7
Brand name: Poseidon
Product recalled: Male Sexual Enhancement Dietary Supplement
Reason of the recall: Undeclared Tadalafil and Sildenafil
FDA Recall date: May 11, 2021
Recall details: Delray Beach, Florida, Yamtun7 is voluntarily recalling all lots of Poseidon Platinu... See Morem 3500 to the consumer level. FDA analysis has found the product to contain undeclared tadalafil and sildenafil. Tadalafil and sildenafil are drugs known as phosphodiesterase (PDE-5) inhibitors found in FDA approved products for the treatment of male erectile dysfunction. The presence of tadalafil and sildenafil in Poseidon Platinum 3500 makes it an unapproved new drug for which the safety and efficacy have not been established and, therefore subject to recall.

Consumers with underlying medical issues who take Poseidon Platinum 3500 with undeclared tadalafil and sildenafil may experience serious 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.

To date, Yamtun7 has not received any reports of adverse events related to this recall. This tainted product is marketed as a dietary supplement for male sexual enhancement and is packaged in a blue pack which contains one single blue pill with blue label and gold text with barcode 0 95842 05876 0. The affected lot numbers include all lots. Poseidon Platinum 3500 was distributed via internet and by eBay at www.ebay.com/usr/yamtun7store from July 1, 2019 to September 28, 2020 to nationwide in the USA.

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. Yamtun7 is notifying its customers by this press announcement and via e-mail of this recall.

Consumers that have Poseidon Platinum 3500, which is being recalled should stop using and destroy them. Consumers with questions regarding this recall can contact Yamtun7 by phone at 561-674-3203 7 days of week from 9 am to 5 pm EDT or e-mail yamtun7@gmail.com. Consumers should contact their physicians or healthcare provider if they have experienced any problems that may be related to taking or using this drug 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. Complete and submit the report Online. Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178. 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
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Reported By SafelyHQ.com User

May 11, 2021 3:01 PM

“Company name: Dash Xclusive
Brand name: Imperia Elita
Product recalled: Vitaccino Coffee weight loss and anxiety dietary supplement
Reason of the recall: Undeclared Sibutramine and Fluoxetine
FDA Recall date: May 11, 2021
Recall details: Glendale, California, Dash Xclusive is voluntarily recal... See Moreling all lots of Imperia Elita Vitaccino Coffee to the consumer level. FDA analysis has found the product to contain undeclared sibutramine and fluoxetine. Sibutramine was an FDA-approved drug used as an appetite suppressant for weight loss but was withdrawn from the market because of safety issues, including stroke, heart failure and serious health risk especially to those with underlying heart related disease.

Fluoxetine is an FDA approved drug indicated for the treatment of various depressive disorders, obsessive compulsive disorder, bulimia and panic disorders. This drug product carries a box warning for suicidal thoughts and behaviors and it needs to be monitored closely by a prescriber. The presence of sibutramine and fluoxetine in Imperia Elita Vitaccino coffee renders it an unapproved drug for which safety and efficacy has not been established and therefore subject to a recall. Dash Xclusive has not received any reports of adverse events related to this recall.

Risk Statement: Products containing undeclared sibutramine pose a threat to consumers because sibutramine is known to substantially increase blood pressure and/or pulse rate in some patients and may present a significant risk for patients with a history of coronary artery disease, congestive heart failure, arrhythmias or stroke. Products containing undeclared fluoxetine could cause suicidal thinking and behavior, an accumulation of high levels of serotonin in the body or neuroleptic malignant syndrome (NMS)-like reactions which is a life-threatening neurological disorder; elevated mood state that can cause higher than normal energy levels, restlessness, decreased need for sleep; abnormal bleeding, and low sodium levels.

The product is marketed  as a dietary supplement for weight loss and is packaged in a black rectangular box and contains fifteen sachets. The affected Imperia Elita Vitaccino coffee lots include all lots. Product was distributed Nationwide in the USA via internet and by ebay at www.ebay.com. 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.

Dash Xclusive is notifying its customers by e-messages on the eBay platform and is arranging for return of all recalled products. Consumers that have Imperia Elita Vitaccino Coffee which is being recalled should stop using/return to Dash Xclusive, 610 S. Verdugo Road, Apt 31, Glendale, California 91205. Consumers with questions regarding this recall can contact Dash Xclusive by e-mail at dashxclusive11@gmail.com on Mondays to Thursdays from 11am to 4pm Pacific Time zone. 

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. 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. Complete and submit the report Online. Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178. 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
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Reported By SafelyHQ.com User

May 12, 2021 8:00 PM

“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 12, 2021
Recall details: Company Announcement Morelia, Michoacán, Mexico, Dibar Nutricional S. de R.L. De C.V. (... See More“Dibar”) is voluntarily recalling 27 lots of DIBAR Labs Hand Sanitizer packaged in 8oz (8-53090-00301-3 UPC) and 16 oz (8-53090-00302-0 UPC) fluid ounce bottles, respectively, to the consumer level. (See products listed in the link below in Table 1 and Label 1). Dibar is also voluntarily recalling 2 lots of ProtectoRx Hand Sanitizer packaged in 2oz (Lot Number LDHSN050720) and 16oz (Lot Number LDHSN050820) fluid ounce bottles, respectively, to the consumer level. (See products listed in the link below in Table 2 and Label 2). 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, scent, and lot code provided in the table at the end of this release. These products were distributed nationwide in the USA through S.E.N.D. LLC and its customers (Click in the link below Table 1). Products labeled as ProtectoRx Hand Sanitizer were distributed in Puerto Rico through PR TRADING LLC and its customers (Click in the link below Table 2.). Dibar Nutricional S. de R.L. De C.V., has notified its direct distributors by a letter with confirmatory email and asked that they remove the recalled products from commerce immediately if they still had any in 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 with questions regarding this recall can contact our Commercial Offices, +52 443-314-5369, M-F, during business hours 9:00 a.m. – 6:00 p.m. ET and/or email us to QA@dibarlabs.com.  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.

- Complete and submit the report Online.
- Regular Mail or Fax: Download form or call 1- 800-332-1088 to request a reporting form, then complete and return to the address on the pre-addressed form, or submit by fax to 1-800-FDA-0178

This recall is being conducted with the knowledge of the U.S. Food and Drug Administration. (Table 1. Lots distributed to S.E.N.D. LLC and its customers)  

Check the full recall details on fda.gov

Source: FDA
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Reported By SafelyHQ.com User

May 13, 2021 2:01 PM

“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,... See Morelot 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
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Reported By SafelyHQ.com User

May 13, 2021 3:03 PM

“Company name: Scentsational Soaps & Candles, Inc.
Brand name: Goose Creek, COCO TKO
Product recalled: Hand Sanitizer
Reason of the recall: Presence of Methanol (Wood Alcohol), Benzene and Acetaldehyde
FDA Recall date: May 13, 2021
Recall details: Scentsational Soaps & Candles, Inc., has volunta... See Morerily expanded its April 27 recall of scented Hand Sanitizers to include three lots of Goose Creek HAND SANITIZER (NDC 75078-004) + Aloe and one lot of COCO TKO HAND SANITIZER in 3.38 and 3.4 fluid ounce spray bottles, respectively, to the consumer level.

These products are listed in the table below. These products are being recalled after testing conducted by our firm revealed the presence of methanol (wood alcohol), benzene, and acetaldehyde. These products were sold on the Internet and distributed nationwide in the USA by Goose Creek Candles, LLC and Coconut Stand.

- Goose Creek HAND SANITZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Blueberry Limeade Anti-Bacterial Spray. UPC or NDC: NO UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe (3.38 fl oz. (100 ml)). Scent: Limoncello Anti-Bacterial Spray. UPC or NDC: NO UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Beach Dreams Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Grape Soda Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Champagne Bubbles Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Dragonfruit Splash Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Marshmallows Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20258. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Melon Picnic Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20259. Retailer and States shipped: 35 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Optimistic Vibes Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20259. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Red White and Blue Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20259. Retailer and States shipped: 42 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Watermelon Lemonade Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20259. Retailer and States shipped: 35 cases shipped on 9/22/20 to KY.
- Goose Creek HAND SANITIZER + Aloe Goose (3.38 fl oz. (100 ml)). Scent: Tropical Daydream Anti-Bacterial Spray. UPC or NDC: No UPC. Lot: 20260. Retailer and States shipped: 36 cases shipped on 9/22/20 to KY.
- COCO TKO HAND SANITIZER (3.4 fl oz. (100.55 ml)). Scent: Coconut Stand. UPC or NDC: No UPC. Lot: 20260. Retailer and States shipped: 14 cases shipped on 9/16/20 to FL.

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. Exposure to benzene can occur through inhalation, oral, and skin.

There is a reasonable probability that benzene present at levels above the maximum daily exposure recommendations can result in cancers including leukemia and blood cancer of the bone marrow and blood disorders which can be life-threatening. Additionally, animal studies have shown that acetaldehyde can possibly cause cancer in humans. 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 five-digit lot code printed on the bottle near the base. The products can be identified by the label, scent, and lot code provided in the table at the end of this release. Photos are also provided at www.scentsational-products.com.

Scentsational Soaps & Candles, Inc. has notified its direct customers by telephone with confirmatory email and asked that they remove the recalled products from commerce immediately if they still had any in 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.

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
See Less
Reported By SafelyHQ.com User

May 13, 2021 11:25 PM

“I ordered that chainsaw from Stihl Gwas..advertised on Facebook on April 17 and still haven't received product. I paid through PayPal and money was taken out a long time ago by them. I want my money back! Get rid of these scammers! ” See Less
Reported By SafelyHQ.com User

May 13, 2021 9:21 PM

“They are a scam. I received the same little chain with two rings. Wish I had googled this item before. BEWARE!!!! See Less
Reported By SafelyHQ.com User

May 13, 2021 8:10 PM

““I ordered the battery powered wood cutter from an advertisement on Facebook and just as everyone else has said, I received a chain on two key rings. My receipt clearly states battery powered wood cutter. The chain was pictured, but I was shown as part of the order, not a choice, or else my receipti... See Mores wrong. They did not send me what I purchased. Good ole bait and switch ” this chain looks like a weapon and I want my money back See Less
Reported By SafelyHQ.com User

Vaccination - J&J Info, Portland, OR, USA

Symptoms: Fever Fatigue Soreness
Portland, OR, USA

May 13, 2021 7:57 PM

“I am a woman in her 50's and I received the J&J vaccine on Monday 05.10.21 felt good right after arm a bit sore. The next day pretty fatigued low grade fever. See Less
Reported By SafelyHQ.com User