FoodMar 6, 2024
The Quaker Oats Co Quaker Chewy Bars Chocolate Chip 8ct 6.7 oz, 18ct 15.1 oz,30ct recall — FDA F-0940-2024
potential Salmonella
Class IIFDA: TerminatedThe Quaker Oats Co.
Monthly breakdown
2024 recalls by month
Select a month to review the recall records reported during that period.
December 2024325 records · 4 categoriesNovember 2024355 records · 4 categoriesOctober 2024409 records · 4 categoriesSeptember 2024547 records · 4 categoriesAugust 2024327 records · 4 categoriesJuly 2024318 records · 4 categoriesJune 2024286 records · 4 categoriesMay 2024422 records · 4 categoriesApril 2024323 records · 4 categoriesMarch 2024332 records · 4 categoriesFebruary 2024425 records · 4 categoriesJanuary 2024298 records · 4 categories
2024 recalls — page 152
Records are ordered by the best available source date.
FoodMar 6, 2024
The Quaker Oats Co Quaker Chewy Bars Chocolate Chip Halloween Minis 28ct 13.8 oz recall — FDA F-0943-2024
potential Salmonella
Class IIFDA: TerminatedThe Quaker Oats Co.
FoodMar 6, 2024
The Quaker Oats Co Quaker Big Chewy Bars Peanut Butter Chocolate Chip 5ct 7.4 oz recall — FDA F-0937-2024
potential Salmonella
Class IIFDA: TerminatedThe Quaker Oats Co.
FoodMar 6, 2024
The Quaker Oats Co Quaker Oatmeal Squares Brown Sugar 14.5 oz recall — FDA F-0989-2024
potential Salmonella
Class IIFDA: TerminatedThe Quaker Oats Co.
FoodMar 6, 2024
Sargento Foods Swiss cheese packaged in the following configurations: 1 recall — FDA F-1011-2024
Listeria monocytogenes
Class IFDA: TerminatedSargento Foods, Inc.
FoodMar 6, 2024
The Quaker Oats Co Cap'n Crunch Treats Peanut Butter Crunch Cereal Bar 0.84 oz 8 recall — FDA F-0983-2024
potential Salmonella
Class IIFDA: TerminatedThe Quaker Oats Co.
FoodMar 6, 2024
The Quaker Oats Co Cap n Crunch Instant Oatmeal 8.5 oz 6 Count recall — FDA F-0996-2024
potential Salmonella
Class IIFDA: TerminatedThe Quaker Oats Co.
FoodMar 6, 2024
The Quaker Oats Co Quaker Chewy Mini Dipps Summer Night S'mores 12ct 8.9 oz Bars recall — FDA F-0959-2024
potential Salmonella
Class IIFDA: TerminatedThe Quaker Oats Co.
FoodMar 6, 2024
The Quaker Oats Co Quaker Chewy Bars Less Sugar Peanut Butter Chocolate Chip 8ct recall — FDA F-0950-2024
potential Salmonella
Class IIFDA: TerminatedThe Quaker Oats Co.
DrugMar 6, 2024
Seatex 7 Eleven FOR GAS ISLAND USE ONLY, Hand Sanitizer, Ethanol 70% v/v Antiseptic recall — FDA D-0358-2024
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Class IIFDA: TerminatedSeatex LLC
DrugMar 6, 2024
Omeprazole and Sodium Bicarbonate For Oral Suspension 40mg/1,680mg, This packet contains recall — FDA D-0355-2024
Subpotent Drug: Out of specification for assay
Class IIFDA: CompletedBausch Health Companies, Inc.
DrugMar 6, 2024
Denver Solutions, LLC DBA Leiters Health Moxifloxacin PF, 1mg/ml, in Sterile Balanced Salt recall — FDA D-0361-2024
Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
Class IIFDA: OngoingDenver Solutions, LLC DBA Leiters Health
DrugMar 6, 2024
Brassica Pharma Pvt CVS Health Lubricant Eye Ointment recall — FDA D-0353-2024
Lack of Assurance of Sterility
Class IIFDA: OngoingBrassica Pharma Pvt Ltd
DrugMar 6, 2024
Denver Solutions, LLC DBA Leiters Health Lidocaine HCL 1% (10mg/mL), PHENYLephrine HCL 1.5% recall — FDA D-0363-2024
Presence of Particulate Matter: glass vials from the manufacturer showed signs of glass delamination.
Class IIFDA: OngoingDenver Solutions, LLC DBA Leiters Health
DrugMar 6, 2024
Seatex PROBLEND Antibacterial Foaming Silk All-In-One Foaming Hand Sanitizer & Cleanser recall — FDA D-0356-2024
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Class IIFDA: TerminatedSeatex LLC
DrugMar 6, 2024
Seatex 7 Eleven Hand Sanitizer Gel, Ethanol 70% v/v Antiseptic, Mountain Spring Scent, 1250 recall — FDA D-0359-2024
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Class IIFDA: TerminatedSeatex LLC
DrugMar 6, 2024
Seatex PROBLEND Hand Sanitizer, Refreshing Gel Hand Sanitizer, Ethanol 70% v/v Antiseptic recall — FDA D-0360-2024
CGMP Deviations: deficiencies were identified during an FDA inspection of Seatex's manufacturing facility.
Class IIFDA: TerminatedSeatex LLC
DrugMar 6, 2024
Fluticasone Propionate Nasal Spray USP, 50 mcg per spray, 120 metered sprays, 16 g net fill recall — FDA D-0349-2024
CGMP Deviations:Suspected potential presence of Burkholderia cepacia complex
Class IIFDA: OngoingGolden State Medical Supply Inc.
DrugMar 6, 2024
Mesalamine Extended-Release Capsules, USP 500mg recall — FDA D-0350-2024
Failed Dissolution Specifications: Out of specification for dissolution.
Class IIFDA: OngoingSUN PHARMACEUTICAL INDUSTRIES Inc.
VehicleMar 5, 2024
Nissan pretensioner recall — NHTSA campaign 24V176000
Nissan North America, Inc. (Nissan) is recalling certain 2024 Pathfinder and Infiniti QX60 vehicles. The lap belt pretensioner in the left-side front seat belt assembly may be improperly…
pretensionerNissan North America, Inc.
Medical DeviceFeb 28, 2024
Boston Scientific EndoVive Replacement Button Kit w/ ENFIT 28F 2.8 CM, Outer Box UPN recall — FDA Z-1153-2024
Affected batches of the kit contain Stoma Measuring Devices sized to measure for an 18/24F replacement button, but are labeled as being for a 28F. Use of defective product may lead to…
Class IIFDA: OngoingBoston Scientific Corporation
Medical DeviceFeb 28, 2024
Voco GmbH IonoStar Plus, Catalog (REF) Numbers: a) 2540, b)2543, c) 2544, d) 2545, e) 2546 recall — FDA Z-1142-2024
Due to an error in the manufacturing process, it is possible that an incorrect plunger has been fitted to some capsules. This plunger does not contain the correct reactive component for…
Class IIFDA: OngoingVoco GmbH
Medical DeviceFeb 28, 2024
Philips Allura Xper Interventional Fluoroscopic X-ray Systems, specifically the DIMMs recall — FDA Z-1156-2024
Dual In-Line Memory Modules (DIMMs) may not perform as intended. System may stop functioning and imaging may not be possible, resulting in delay of procedure.
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceFeb 28, 2024
3M Company - Health Care Business 3M Specialty Blade Assembly, REF 9660,70-2011-8491-1 recall — FDA Z-1170-2024
3M has added the following cautionary statement regarding the use of the product: "Caution - To reduce the risk of burns, which if not avoided may result in minor injury: " Do not use on…
Class IIFDA: Ongoing3M Company - Health Care Business
About the 2024 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.