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Safety Reports: Recall

Updated:

Real Time Reports

Botanical-Be is voluntarily recalling all lots of Kuka Flex Forte, Capsules, Artri King, Capsules, and Reumo Flex, Capsules to the consumer level. FDA analysis has found these capsules, to be tainted with Diclofenac. Diclofenac is an approved non-steroidal anti-inflammatory drug (NSAID), the presence of Diclofenac in Kuka… See more

#vitamins #drugs #recall #unitedstates

312   Comments Comment
TFP Nutrition of Nacogdoches, TX announced today that it is issuing a voluntary recall of Retriever All Life Stages Mini Chunk Chicken Recipe Dry Dog Food due to potential Salmonella contamination. Salmonella can affect animals eating the products and there is risk to humans from handling contaminated… See more

#recall #dogfood #petfood #unitedstates

The FDA is cautioning pet owners not to feed their pets certain lots of Darwin's Natural Pet Products raw cat and dog food after product samples tested positive for Salmonella. These products are manufactured by Arrow Reliance Inc., doing business as Darwin's Natural Pet Products, and are… See more

#raw #recall #petfood #unitedstates

312   Comments Comment
The FSAI announced the recall of MountainGrown.ie Irish CBD Oil due to the presence of unsafe levels of delta-9-tetrahydrocannabinol (∆9THC) in excess of the European Food Safety Authority (EFSA) acute reference dose. This product was distributed in Ireland.

The recalled product is:
- MountainGrown.ie Irish CBD Oil;… See more

#cbd #recall #ireland

FDA announced the recall of Hollywood Feed Carolina Made Jerky Treats by Carolina Prime Pet, Inc due to potential salmonella contamination. All products were shipped to one customer in Tennessee.

The recalled products are:
- Hollywood Feed CAROLINA Made USA FARM RAISED BEEF JERKY NET WEIGHT 5OZ… See more

#recall #petfood #tennessee #unitedstates

107   Comments Comment
Family Dollar is initiating a voluntary retail-level product recall of certain over-the-counter drugs and medical devices regulated by the U.S. Food and Drug Administration (FDA). These items were stored outside of labeled temperature requirements by Family Dollar and inadvertently shipped to certain stores on or around June… See more

#medicaldevices #drugs #recall #familydollar #unitedstates

312   Comments Comment
KVK-Tech, Inc. is voluntarily recalling one lot (Batch Number: 17853A; "the batch") of Betaxolol Tablets, USP 10 mg, White, Round, film coated biconvex tablets, debossed "K" above bisect "13" on one side and plain on the other side" to the consumer level. The batch was distributed nationwide… See more

#recall #drugs #unitedstates

312   Comments Comment
Hospira, Inc., a Pfizer company, is voluntarily recalling 4.2% Sodium Bicarbonate Injection, USP, 5 mEq/10mL vial; 1% Lidocaine HCl Injection, USP, 50 mg/5mL vial; and 2% Lidocaine HCl Injection, USP, 100 mg/5mL vial to the user level due to the potential presence of glass particulate matter. To… See more

#blood #recall #drugs #unitedstates

312   Comments Comment
Biomic Sciences is voluntarily recalling all lots of ION* Sinus Support, ION* Biome Sinus, and Restore Sinus Spray products to the consumer level. FDA testing found the product to contain microbial contamination identified as Microbacterium sp., Fictibacillus sp., Bacillus sp., (primarily B. malikii), and Paenibacillus sp (these… See more

#recall #drugs #unitedstates

312   Comments Comment
Merck Animal Health, known as MSD Animal Health outside of the United States and Canada, a division of Merck & Co., Inc., Rahway, N.J., USA (NYSE:MRK), is voluntarily recalling 4 additional batches of BANAMINE® / BANAMINE®-S (flunixin meglumine injection) 50 mg/mL in the United States, used for… See more

#drugs #recall #unitedstates

312   Comments Comment