FoodSep 7, 2022
Lyons Magnus High Protein, Nutritional Drink recall — FDA F-1613-2022
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Class IFDA: TerminatedLyons Magnus, Inc.
Monthly breakdown
2022 recalls by month
Select a month to review the recall records reported during that period.
December 2022318 records · 4 categoriesNovember 2022270 records · 4 categoriesOctober 2022288 records · 4 categoriesSeptember 2022318 records · 4 categoriesAugust 2022293 records · 4 categoriesJuly 2022334 records · 4 categoriesJune 2022348 records · 4 categoriesMay 2022227 records · 4 categoriesApril 2022205 records · 4 categoriesMarch 2022449 records · 4 categoriesFebruary 2022237 records · 4 categoriesJanuary 2022296 records · 4 categories
2022 recalls — page 50
Records are ordered by the best available source date.
FoodSep 7, 2022
Clinical Innovations Sweetums 24% sucrose solution with preservative recall — FDA F-1685-2022
Firm received complaints of leaking, black liquid, and black particulates in the product vials.
Class IIFDA: TerminatedClinical Innovations, LLC
FoodSep 7, 2022
Lyons Magnus Aloha Organic Protein Drink, Chocolate Sea Salt, Plant-based recall — FDA F-1603-2022
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Class IFDA: TerminatedLyons Magnus, Inc.
FoodSep 7, 2022
Lyons Magnus Sysco Imperial Med Plus 2.0 butter Pecan Nutritional Drink recall — FDA F-1634-2022
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Class IFDA: TerminatedLyons Magnus, Inc.
FoodSep 7, 2022
Lyons Magnus kate farms Peptide 1.5 Cal/mL, Plain, Sole-Source Nutrition recall — FDA F-1671-2022
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Class IFDA: TerminatedLyons Magnus, Inc.
DrugSep 7, 2022
Tsm Brands Luxury 70% Isopropyl Alcohol, First Aid Antiseptic with Wintergreem12 FL recall — FDA D-1475-2022
Labeling: Product Contains Undeclared API - product contains undeclared ethyl alcohol
Class IIFDA: OngoingTsm Brands LLC
DrugSep 7, 2022
Family Dollar Stores, LLC Colgate Anticavity Fluoride Toothpaste, OPTIC WHITTE RENEWAL, 3% recall — FDA D-1466-2022
cGMP deviation: Product held outside of appropriate temperature storage conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugSep 7, 2022
Family Dollar Stores, LLC Colgate Anticavity Fluoride Toothpaste OPTIC WHITE STAIN FIGHTER recall — FDA D-1469-2022
cGMP deviation: Product held outside of appropriate temperature storage conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugSep 7, 2022
Family Dollar Stores, LLC Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE ADVANCED ICY recall — FDA D-1467-2022
cGMP deviation: Product held outside of appropriate temperature storage conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugSep 7, 2022
Triamcinolone Acetonide Cream USP, 0.1%, 80 g tube recall — FDA D-1497-2022
CGMP Deviations: Product complaints reporting the product to have a gritty texture and lack of effectiveness.
Class IIFDA: TerminatedPadagis US LLC
DrugSep 7, 2022
Family Dollar Stores, LLC Colgate Whitening Mouthwash, OPTIC WHITE ICY FRESH MINT. 16 fl recall — FDA D-1470-2022
cGMP deviation: Product held outside of appropriate temperature storage conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugSep 7, 2022
Neomycin Sulfate Tablets, USP 500 mg , 100-count bottles recall — FDA D-1473-2022
CGMP Deviations: A foreign matter identified as teflon was found in the Active Pharmaceutical Ingredient (API) used in the manufacture of Neomycin Sulfate Tablets, USP 500 mg.
Class IIFDA: TerminatedTeva Pharmaceuticals USA Inc.
DrugSep 7, 2022
Akorn Timolol Maleate Ophthalmic Solution, USP, 0.5%, 5 x 0.3 mL Single-Dose Vials recall — FDA D-1471-2022
Failed Impurities/Degradation Specifications: Identification of an unknown impurity at the 12-month stability point.
Class IIIFDA: OngoingAkorn, Inc.
DrugSep 7, 2022
Family Dollar Stores, LLC Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE with CHARCOAL recall — FDA D-1468-2022
cGMP deviation: Product held outside of appropriate temperature storage conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugSep 7, 2022
Family Dollar Stores, LLC Colgate Anticavity Fluoride Toothpaste, OPTIC WHITE PRO SERIES recall — FDA D-1465-2022
cGMP deviation: Product held outside of appropriate temperature storage conditions.
Class IIFDA: OngoingFamily Dollar Stores, LLC.
DrugSep 7, 2022
LNK International Nighttime Sleep-Aid (doxylamine succinate HCl) tablets, 25 mg, 48-count recall — FDA D-1472-2022
Labeling: Not Elsewhere Classified: Carton incorrectly identifies product as doxylamine succinate HCl, however the product is doxylamine succinate.
Class IIIFDA: TerminatedLNK International, Inc.
VehicleSep 7, 2022
Nissan automatic transmission recall — NHTSA campaign 22V671000
Nissan North America, Inc. (Nissan) is recalling certain 2020-2023 Titan, 2020-2022 Frontier, and 2023 Z vehicles. The transmission parking pawl may not engage when the vehicle is shifted…
automatic transmissionNissan North America, Inc.
VehicleSep 1, 2022
Rogue buckle recall — NHTSA campaign 22V666000
Nissan North America, Inc. (Nissan) is recalling certain 2021-2022 Rogue vehicles. The rear seat belts for the left-hand and right-hand rear seats may not retract properly. As such, these…
buckleNissan North America, Inc.
Medical DeviceAug 31, 2022
Mckesson Medical-Surgical Inc. Corporate Office a. Alcon Clear Care Contact Lens Solution recall — FDA Z-1590-2022
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between…
Class IIFDA: OngoingMckesson Medical-Surgical Inc. Corporate Office
Medical DeviceAug 31, 2022
Mckesson Medical-Surgical Inc. Corporate Office Dynarex SWAB, LEMON GLYCERIN recall — FDA Z-1634-2022
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between…
Class IIFDA: OngoingMckesson Medical-Surgical Inc. Corporate Office
Medical DeviceAug 31, 2022
Mckesson Medical-Surgical Inc. Corporate Office MORRISON MEDICAL Morrison Medical OB KIT recall — FDA Z-1632-2022
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between…
Class IIFDA: OngoingMckesson Medical-Surgical Inc. Corporate Office
Medical DeviceAug 31, 2022
Mckesson Medical-Surgical Inc. Corporate Office 3M COMPANY 3M PAD, GROUNDING SAFETY RING recall — FDA Z-1608-2022
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between…
Class IIFDA: OngoingMckesson Medical-Surgical Inc. Corporate Office
Medical DeviceAug 31, 2022
Mckesson Medical-Surgical Inc. Corporate Office Fischer Cone Biopsy Excisor EXCISOR, CONE recall — FDA Z-1612-2022
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between…
Class IIFDA: OngoingMckesson Medical-Surgical Inc. Corporate Office
Medical DeviceAug 31, 2022
Medtronic Neuromodulation Vanta Clinician Programmer Application, Model A71200 recall — FDA Z-1571-2022
Potential for Vanta Clinician Programmer Application (CP App) A71200 v2.0.2455 to display an Unexpected Device Error Code 1502 Message, and the user will be unable to perform programming of…
Class IIFDA: OngoingMedtronic Neuromodulation
About the 2022 recall archive
This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.