FoodSep 7, 2022
Lyons Magnus The Original Oatly! Oat-Milk Barista Edition recall — FDA F-1673-2022
Findings and potential for Cronobacter sakazakii and Clostridium botulinum.
Class IFDA: TerminatedLyons Magnus, Inc.
Latest records
Latest recalls — page 687
The newest recall records with useful source details are listed here.
FoodSep 7, 2022
Clinical Innovations Sweetums 24% Sucrose Solution Preservative Free 15 mL cups recall — FDA F-1682-2022
Firm received complaints of leaking cups, black liquid, and black particulates in the 24% Sucrose Solution.
Class IIFDA: TerminatedClinical Innovations, LLC
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.
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
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Recent recall archives
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October 2026110 records · 3 categoriesSeptember 2026364 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories