Complete FDA and NHTSA recall records dated in February 2018.
These records include useful source details for the selected month.
Marketed Without An Approved NDA/ANDA: Flawless Beauty, LLC is voluntarily recalling all lots of different products sold individually or as part of multi-unit kits in accordance with…
Products may contain undeclared soy lecithin.
Products have the potential to be contaminated with Listeria monocytogenes.
The firm received Ice Oatmeal Cookies that actually contain Coconut Macaroon Cookies. Product is being recalled due to mislabeling. Product contains both milk and tree nuts that are not…
A higher than normal micro result was found at the six month time point for one lot of Liquid L-Carnitine.
Product is labeled as Tonkotsu, but the actual flavor packet inside is Assari Shoyu , which contains a fish (sardines).
Rapid Alert System for Food and Feed notification received from Italy regarding high histamine levels in imported anchovy sauce.
Products have the potential to be contaminated with Listeria monocytogenes.
Firm determined that their Rice Cake Soup has undeclared milk in the form of sodium caseinate.
Kvas, a fermented non-alcoholic drink, due to bulging. A hole was punched to the lids of the gallon plastic jugs to prevent the plastic jugs from bulging. The package integrity was…
Claudio Specialty Foods is recalling anchovy sauce after receiving a telephone call from their supplier notifying them that the product was found to contain high levels of histamine.
A consumer purchased who purchased a labeled Coat & Bake Chicken but actually contained Pork Seasoning. The Pork Seasoning product contains the major food allergen "Milk" not declared on…
Products have the potential to be contaminated with Listeria monocytogenes.
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products…
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Marked Without An Approved NDA/ANDA: FDA analysis found these products to contain sildenafil, an FDA approved drug for the treatment of erectile dysfunction, making these products…
Subpotent Drug:The titratable iodine contained in the Povidone-Iodine prep pads is below label claim of 0.85%.
Use this page to compare the recalls reported during the month, then open an individual record for the exact reason, classification, company, remedy or distribution information available from the official source. Monthly counts are descriptive, not a safety rating.
