FoodJan 5, 2022
Slayer Forever, LLC dba BUBS Naturals BUBS Naturals Fountain of Youth Formula recall — FDA F-0354-2022
Supplement contains undeclared milk from MCT oil powder ingredient.
Class IFDA: TerminatedSlayer Forever, LLC dba BUBS Naturals
January 2022 recalls — page 13
These records include useful source details for the selected month.
FoodJan 5, 2022
Giant Eagle 10 oz recall — FDA F-0355-2022
Giant Eagle, Inc., Pittsburgh, PA has initiated a recall of Giant Eagle Diced Green Peppers, 10 oz. 283 g, Frozen bag, 12 packages per case, Best By 10/14/2023 because the product tested…
Class IIFDA: TerminatedGiant Eagle, Inc.
FoodJan 5, 2022
Frozen Food Development Giant Eagle, Diced Green Peppers, 10 oz recall — FDA F-0356-2022
Frozen Food Development, Lancaster, PA is initiating a recall of Giant Eagle, Diced Green Peppers, 10 oz. poly bags and 22# cases (12/10 oz. bags per case) and bulk 22 lbs. bags because…
Class IIFDA: TerminatedFrozen Food Development
DrugJan 5, 2022
Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL) recall — FDA D-0295-2022
Superpotent Drug
Class IFDA: OngoingTeligent Pharma, Inc.
DrugJan 5, 2022
Lidocaine Hydrochloride, Topical Solution USP, 4% (40 mg/mL) recall — FDA D-0296-2022
Superpotent Drug: Minimally superpotent
Class IIFDA: OngoingTeligent Pharma, Inc.
DrugJan 5, 2022
Teligent Pharma Betamethasone Dipropionate Lotion USP, 0.05% (Augmented), 30 mL bottle recall — FDA D-0297-2022
Failed Stability Specifications: lot did not meet specification for the Active Pharmaceutical Ingredient (API) particle test, which was determined through routine stability testing
Class IIFDA: TerminatedTeligent Pharma, Inc.
DrugJan 5, 2022
Valisa MFG kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles recall — FDA D-0363-2022
Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol making it an unapproved new drug and contains methanol
Class IFDA: TerminatedValisa MFG LLC
DrugJan 5, 2022
Aroma Release Technologies Klean Touch Hand Sanitizer (Ethyl Alcohol 70%) Ingredients recall — FDA D-0298-2022
Marketed Without an Approved NDA/ANDA: Product labeled to contain methanol making it an unapproved new drug and contains methanol
Class IFDA: TerminatedAroma Release Technologies Inc.
How to use this monthly recall archive
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.