FoodFeb 21, 2024
UNFI General Corporate Woodstock 5 Grain Cereal recall — FDA F-0872-2024
The ingredient Triticale is not identified as wheat.
Class IIFDA: TerminatedUNFI General Corporate
Latest records
Latest recalls — page 438
The newest recall records with useful source details are listed here.
FoodFeb 21, 2024
Lydia Pack 3 Al Amir Fresh Foods Harissa Spicy Hummus With a Kick, packaged recall — FDA F-0868-2024
Hummus product label declares Tahini but does not declare sesame.
Class IFDA: TerminatedLydia Pack 3 Inc.
FoodFeb 21, 2024
Fresh Express Incorpated Chopped Salad Kit Southwest with condiments recall — FDA F-0875-2024
Product has the potential to be contaminated with Listeria monocytogenes. The condiment pack in the salad kit contains cheese recalled by the cheese supplier.
Class IFDA: TerminatedFresh Express Incorpated
FoodFeb 21, 2024
U.S. Tov Dragonfly Jelly Bar Handbag 11.64oz, 17.63oz UPC Code recall — FDA F-0865-2024
Potential choking hazard; product contains konjac.
Class IFDA: TerminatedU.S. Tov, Inc.
FoodFeb 21, 2024
Lydia Pack 3 Al Amir Fresh Foods Classic Hummus Creamy Garbanzo, packaged recall — FDA F-0867-2024
Hummus product label declares Tahini but does not declare sesame.
Class IFDA: TerminatedLydia Pack 3 Inc.
VehicleFeb 21, 2024
Toyota Motor Engineering & Manufacturing display function recall — NHTSA campaign 24V124000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2023 Mirai, Lexus LS500, LS500H, 2023-2024 Lexus ES250, ES300H, ES350, 2024 Lexus LC500, and LC500H vehicles equipped…
display functionToyota Motor Engineering & Manufacturing
VehicleFeb 21, 2024
Toyota Motor Engineering & Manufacturing seats recall — NHTSA campaign 24V128000
Toyota Motor Engineering & Manufacturing (Toyota) is recalling certain 2023-2024 Camry and Camry Hybrid vehicles. The second-row center and right-side seats may have insufficiently welded…
seatsToyota Motor Engineering & Manufacturing
DrugFeb 21, 2024
Nortrel 7/7/7 recall — FDA D-0322-2024
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
Class IIIFDA: OngoingTeva Pharmaceuticals USA, Inc.
DrugFeb 21, 2024
The Harvard Drug Group LLC dba Major HydrALAZINE Hydrochloride Tablets, USP 10mg recall — FDA D-0324-2024
an out of specification result obtained during routine stability testing for Impurities. There is a remote possibility that use of this product could cause a medically reversible or…
Class IIFDA: TerminatedThe Harvard Drug Group LLC dba Major Pharmaceuticals…
DrugFeb 21, 2024
IntegraDose Compounding Services Vasopressin 2 Units/2 mL in 0.9% Sodium Chloride Sterile recall — FDA D-0325-2024
Sub-potent drug: failure to maintain potency through the duration of the labeled expiration/beyond-use date.
Class IIFDA: OngoingIntegraDose Compounding Services LLC
DrugFeb 21, 2024
Nortrel recall — FDA D-0321-2024
Discoloration: discolored tablets (shades of blue) mixed in with the white inert remainder tablets.
Class IIIFDA: OngoingTeva Pharmaceuticals USA, Inc.
VehicleFeb 15, 2024
Chrysler defroster/defogger/hvac system recall — NHTSA campaign 24V111000
Chrysler (FCA US, LLC) is recalling certain 2021-2024 Jeep Wrangler and 2022-2024 Jeep Grand Cherokee vehicles. A hybrid control processor (HCP) software error may cause the defrosting and…
defroster/defogger/hvac systemChrysler (FCA US, LLC)
VehicleFeb 15, 2024
Honda steering recall — NHTSA campaign 24V114000
Honda (American Honda Motor Co.) is recalling certain 2023-2024 Odyssey and 2024 Acura RDX vehicles. The steering gear box assembly may not have been tightened properly, allowing water to…
steeringHonda (American Honda Motor Co.)
Medical DeviceFeb 14, 2024
Cardinal Health Monoject, 60 mL Syringe Luer-Lock Tip Soft Pack, REF 1186000777T recall — FDA Z-0857-2024
Cardinal Health is expanding their previous product correction actions to a product removal of all sizes of Cardinal Health brand Monoject sterile Syringe Luer-Lock (1, 3, 6, 12, 20, 35,…
Class IFDA: OngoingCardinal Health 200, LLC
Medical DeviceFeb 14, 2024
Becton Dickinson & Co BD BBL Sensi Disc Clarithromycin- 15 ug, used for semi-quantitative in recall — FDA Z-1028-2024
There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or…
Class IIFDA: OngoingBecton Dickinson & Co.
Medical DeviceFeb 14, 2024
Becton Dickinson & Co BD BBL Sensi Disc Ampicillin with Sulbactam 10/10 ¿g, Catalog Number recall — FDA Z-1013-2024
There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or…
Class IIFDA: OngoingBecton Dickinson & Co.
Medical DeviceFeb 14, 2024
Becton Dickinson & Co BD BBL Sensi Disc Doripenem- 15 ug, used for semi-quantitative in recall — FDA Z-1029-2024
There is a possibility of reproducibility, accuracy, and/or QC failures in antibiotic susceptibility testing (AST) for H. influenzae. This may cause product discard, delayed results, or…
Class IIFDA: OngoingBecton Dickinson & Co.
Medical DeviceFeb 14, 2024
Maquet Medical Systems USA BEQ-RF-32-USA RotaFlow Centrifugal Pump with BIOLINE Coating recall — FDA Z-0977-2024
Nonconformities at their seal could potentially compromise the sterile barrier for affected products. Breach of sterile barrier could expose patients to pathogenic agents, resulting in the…
Class IIFDA: OngoingMaquet Medical Systems USA
Medical DeviceFeb 14, 2024
Philips Ingenia Elition X (Product Number 781358) - HA FlexTrak II recall — FDA Z-0974-2024
Magnetic materials were used for the wheels of trolley. Wheels with magnetic material might be attracted to MRI systems if the wheels are in the magnetic field.
Class IIFDA: OngoingPhilips North America
Medical DeviceFeb 14, 2024
Getinge Usa Sales Flow-i C40 Anesthesia System, model 6677400 recall — FDA Z-0989-2024
Potential cybersecurity vulnerability that could lead to a Denial of Service (DoS) attack, tampering, or remote code execution via remote login to the Flow Anesthesia System, any of which…
Class IIFDA: OngoingGetinge Usa Sales Inc.
Medical DeviceFeb 14, 2024
Cardinal Health Monoject, 35 mL Syringe Luer-Lock Tip Soft Pack, REF 1183500777 recall — FDA Z-0856-2024
Cardinal Health is expanding their previous product correction actions to a product removal of all sizes of Cardinal Health brand Monoject sterile Syringe Luer-Lock (1, 3, 6, 12, 20, 35,…
Class IFDA: OngoingCardinal Health 200, LLC
Medical DeviceFeb 14, 2024
PHILIPS MEDICAL SYSTEMS Spectral CT on Rails: Software Version 5.1.0.X, model 728334 recall — FDA Z-1054-2024
A software issue that can incorrectly label all captured images that may lead to misdiagnosis and subsequent incorrect treatment.
Class IIFDA: OngoingPHILIPS MEDICAL SYSTEMS
Medical DeviceFeb 14, 2024
BALT USA The Prestige Coil System is a product family of embolic coils with associated recall — FDA Z-1042-2024
Discoloration was identified along the delivery pusher which was attributed to corrosion of the hypotube. The material which caused the corrosion was identified as remnants of solder flux…
Class IIFDA: OngoingBALT USA, LLC
Medical DeviceFeb 14, 2024
Siemens Healthcare Diagnostics Total immunoglobulin M (IgM total) IVD, kit recall — FDA Z-1003-2024
Potential for a negative bias with quality control (QC) and patient sample results when using the Atellica CH Immunoglobulin M_2 (IgM_2) reagent.
Class IIFDA: OngoingSiemens Healthcare Diagnostics, Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
September 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 categoriesOctober 2025455 records · 4 categories