FoodNov 20, 2024
Westby Cooperative Creamery UPC 7 50388-30105 2 recall — FDA F-0124-2025
Cheese curds may be contaminated with generic E. coli.
Class IIFDA: TerminatedWestby Cooperative Creamery
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 23
Records are ordered by the best available source date.
FoodNov 20, 2024
JR Simplot Company Item #473015 Simplot seasoned CRISP Delivery+ Savory 6 Cut recall — FDA F-0132-2025
Undeclared wheat. Product contains wheat but was mis-labeled as Savory 6 Cut Crinkle Cut Wedge and label does not declare wheat.
Class IIFDA: TerminatedJR Simplot Company
DrugNov 20, 2024
Trinity Gold Nutrition, 60 Capsule, 30 day Supply recall — FDA D-0042-2025
Marketed without an Approved NDA/ANDA: FDA analysis found product to be tainted with undeclared acetaminophen, diclofenac and phenylbutazone.
Class IIFDA: OngoingTrinity Gold Nutrition
DrugNov 20, 2024
The Harvard Drug Group LLC dba Major Hydralazine HCl Tablets, USP, 25mg recall — FDA D-0045-2025
Failed Impurities/Degradation Specifications; during routine stability testing for impurities.
Class IIIFDA: TerminatedThe Harvard Drug Group LLC dba Major Pharmaceuticals…
VehicleNov 20, 2024
Hyundai Motor wiring recall — NHTSA campaign 24V877000
Hyundai Motor America (Hyundai) is recalling certain 2025 Tucson and Santa Cruz vehicles. The console extension wiring assembly may be routed improperly, allowing the transmission to be…
wiringHyundai Motor America
VehicleNov 19, 2024
Jeep Wrangler wiring recall — NHTSA campaign 24V871000
Chrysler (FCA US, LLC) is recalling certain 2024 Jeep Wrangler vehicles. The incorrect dash wiring harness was installed, which can result in inoperative trailer lighting. As such, these…
wiringChrysler (FCA US, LLC)
VehicleNov 14, 2024
Honda critical fasteners recall — NHTSA campaign 24V859000
Honda (American Honda Motor Co.) is recalling certain 2023-2024 Honda Accord, Accord Hybrid, Civic Sedan, Civic Hatchback, Pilot, and 2024 HR-V, Acura Integra and Acura Integra Type S…
critical fastenersHonda (American Honda Motor Co.)
Medical DeviceNov 13, 2024
Biocare Medical intelliPATH Universal HRP Detection Kit, REF: IPK5011G80, containing DAB recall — FDA Z-0315-2025
Kits containing the DAB chromogen buffer, intended for use in either manual or automated Immunohistochemistry (IHC) staining protocols, may produce weak to no staining, which may lead to…
Class IIFDA: OngoingBiocare Medical, LLC
Medical DeviceNov 13, 2024
Beckman Coulter The Access Cortisol assay is a paramagnetic particle, chemiluminescent recall — FDA Z-0313-2025
The Access Cortisol assay protocol file (APF) applies an incorrect calibration curve acceptance parameter at the S1 calibrator level that can lead to a high rate of calibration failures…
Class IIFDA: OngoingBeckman Coulter, Inc.
Medical DeviceNov 13, 2024
DeRoyal C-SECTION TRACEPACK, REF 89-9338-06 recall — FDA Z-0306-2025
DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil…
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceNov 13, 2024
SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION The FLUOROspeed is intended to be used as a recall — FDA Z-0317-2025
X-ray R/F system software with certain versions of the control board may occasionally fail to display images when switching from Fluoroscopy mode to Radiography mode, which may lead to the…
Class IIFDA: OngoingSHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
Medical DeviceNov 13, 2024
Medtronic DLP Aortic Root Cannula with Flow-Guard, REF 11012 recall — FDA Z-0289-2025
There is the potential for a potential sterility breach for three lots of the DLP Aortic Root Cannula due to a misaligned seal
Class IIFDA: OngoingMedtronic Perfusion Systems
Medical DeviceNov 13, 2024
Baxter Healthcare Hillrom Welch Allyn XScribe Cardiac Stress Testing System recall — FDA Z-0325-2025
There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS))…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceNov 13, 2024
Baxter Healthcare Hillrom Welch Allyn HScribe Holter System recall — FDA Z-0320-2025
There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS))…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceNov 13, 2024
Iotamotion iotaSOFT Plus Drive Unit, REF IM-05 recall — FDA Z-0288-2025
Incorrect GTIN number.
Class IIIFDA: CompletedIotamotion Inc.
Medical DeviceNov 13, 2024
Baxter Healthcare Hillrom Welch Allyn RScribe 12-Lead Electrocardiograph System recall — FDA Z-0322-2025
There is the potential for exam files being assigned duplicate Unique Identifiers (UIDs),. If the system receiving the DICOM file (e.g., Picture Archiving and Communication System (PACS))…
Class IIFDA: OngoingBaxter Healthcare Corporation
Medical DeviceNov 13, 2024
Siemens Healthcare Diagnostics epoc BGEM BUN Test Card (25 pk) for the epoc Blood Analysis recall — FDA Z-0286-2025
Siemens Healthcare Diagnostics Inc. has confirmed that a negative sodium bias may exist in one lot of epoc BGEM BUN Test Cards approximately 2 months prior to expiration. The observed…
Class IIFDA: OngoingSiemens Healthcare Diagnostics Inc.
Medical DeviceNov 13, 2024
Elekta Disposable Biopsy Needle Kit for Leksell Stereotactic System, REF 911933, Diameter / recall — FDA Z-0227-2025
Elekta has become aware that Disposable Biopsy Needles can contain some microscopic debris on the inside of the biopsy needle. The material in the debris is stainless steel, same material…
Class IFDA: OngoingElekta Instrument AB
Medical DeviceNov 13, 2024
Canon Medical System, USA Cartesion Prime, Digital PET-CT, Model: PCD-1000A/3D.004 recall — FDA Z-0284-2025
When PET-CT system is executing reconstruction, if PET acquisition for another patient is performed (or PET reconstruction for another patient is performed from raw data processing), PET…
Class IIFDA: OngoingCanon Medical System, USA, Inc.
Medical DeviceNov 13, 2024
GE Healthcare Centricity Universal Viewer Zero Footprint, Model Numbers: 1) 2089507-083 recall — FDA Z-0318-2025
GE HealthCare has become aware of an issue in Centricity Universal Viewer Zero Footprint Client (ZFP) where there is a potential security vulnerability which could allow a malicious actor…
Class IIFDA: OngoingGE Healthcare
Medical DeviceNov 13, 2024
SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION SONIALVISION G4 is a multi-purpose X-ray R/F recall — FDA Z-0316-2025
X-ray R/F system software with certain versions of the control board may occasionally fail to display images when switching from Fluoroscopy mode to Radiography mode, which may lead to the…
Class IIFDA: OngoingSHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION
Medical DeviceNov 13, 2024
DeRoyal CHILDREN'S GENERAL TRACEPACK, REF 89-9342-06 recall — FDA Z-0307-2025
DeRoyal is recalling certain lots of surgical procedure pack products that contain a Stryker SafeAir Smoke Evacuation Pencil. The recall is due to Stryker receiving reports that the pencil…
Class IIFDA: OngoingDeRoyal Industries Inc.
Medical DeviceNov 13, 2024
Ethicon Coated VICRYL Polyglactin 910 Suture VIO 36IN(90CM) USP0(M3.5) S/A CT, Product recall — FDA Z-0319-2025
Complaints were received regarding needle pull-off and suture degradation. Analysis on returned product from this lot confirmed that some sutures were visually degraded in the package.
Class IIFDA: OngoingEthicon, Inc.
Medical DeviceNov 13, 2024
Datascope MEGA 7.5Fr. 40cc Intra-Aortic Balloon with Accessories, Model Number 0684-00 recall — FDA Z-0311-2025
There is discrepant labeling on the inner and outer packaging of the device.
Class IIFDA: OngoingDatascope Corp.
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.