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.
Latest records
Latest recalls — page 433
The newest recall records with useful source details are listed here.
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
Medical DeviceFeb 28, 2024
Baxter Exactamix Pro 2400, REF EXM24DY recall — FDA Z-1002-2024
An error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in redundant…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceFeb 28, 2024
Baxter Exactamix Pro 1200, REF EXM12DY recall — FDA Z-1001-2024
An error was identified in software versions 2.0.8 and 2.1.8 while using the "Use Some Overfill" feature which may lead to over-delivery of an ingredient. This issue can result in redundant…
Class IFDA: OngoingBaxter Healthcare Corporation
Medical DeviceFeb 28, 2024
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V Azurion 5 with a Certeray generator-To perform image recall — FDA Z-1177-2024
Generator may fail due to a potential short circuit in the Printed Circuit Board Assembly (PCBA) in PoInt EVR (Power Invertor). If a short circuit occurs, it will cause the fuses to trip…
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Medical DeviceFeb 28, 2024
AMD Medicom HENRY SCHEIN CRITERION ANTI-FOG EARLOOP MASKS LEVEL 3 (BLUE) recall — FDA Z-1147-2024
Level 3 masks were produced on alternate non-validated production equipment that were not included as part of the initial qualification of the products.
Class IIFDA: OngoingAMD Medicom Inc.
Medical DeviceFeb 28, 2024
Cardinal Health 200 Dover" 100% SILICONE FOLEY TRAY, NEEDLELESS, 14 FR (4.7 MM), 5 CC, 2000 recall — FDA Z-1052-2024
Convenience kits were manufactured and distributed with components which were subsequently recalled by Nurse Assist.
Class IFDA: OngoingCardinal Health 200, LLC
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