Recalls

All US Product Recalls

Searchable archive of product recalls from the FDA, USDA FSIS, CPSC, NHTSA, and EPA — translated into plain English, severity-scored from objective criteria, and always linked back to the original government notice.

How to read this listing

Every recall on this list has been scored 1–5 against an objective rubric from the agency’s own classification, presence of reported injuries or deaths, distribution scope, and hazard type. The colored severity badge on each card is the score — 5 (Critical) means the agency’s own highest classification or reported deaths or serious injuries, 4 (Severe) means significant injury or hospitalization risk, and 3 (High) means a known hazard with no confirmed harm yet. Filter to 3+ (High and above) if you want to skip routine Class-III notices.

The agency chips above control which streams are visible. FDA spans food, drugs, and medical devices. USDA FSIS is meat, poultry, and processed egg products. CPSC is household consumer products. NHTSA is vehicles, tires, and child seats. Nationwide on a card means the recall affects every US state — most do — while a state list means distribution was limited.

Click any recall to see the full summary, affected lot codes and model numbers, the agency’s own classification, and a direct link back to the original government notice for verification.

Agency

All agencies FDA (Food)FDA (Drugs)FDA (Devices)USDA FSIS CPSC NHTSA EPA

27826–27850 of 90165

HighFDA (Devices)·Z-0277-2022·2021-12-01
CT imaging system ceiling mount bracket shaft wear may cause equipment to fall
A CT fluoroscopy imaging system ceiling mount's bracket shaft may wear excessively and go undetected, potentially causing the bracket to detach and fall, risking injury to patients, operators, or service personnel.
Product
Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - CT Vision ACQSIM CT System Number: 728209 Continuous CT (CCT) is a CT or PET/CT product option that enables physicians and radiologists to produce real-time CT images to facilitate image-guided surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0280-2022·2021-12-01
Philips CT Fluoroscopy Ceiling Mount Bracket Wear and Detachment Hazard
Philips Continuous CT Fluoroscopy ceiling mounts may experience monitor bracket assembly wear that goes undetected, potentially causing the bracket to detach and fall on patients, operators, or bystanders during surgery.
Product
Continuous CT Fluoroscopy DVI Ceiling Mount - CCT Arm DVI Option - Gemini TF 16 System Number: 882470 Continuous CT (CCT) is a CT or PET/CT product option that enables physicians and radiologists to produce real-time CT images to facilitate image-guided surgery.
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·21C005000·2021-12-01
Clek Recalls Foonf and Fllo Convertible Child Seats for Foam Choking Hazard
Clek is recalling specific Foonf and Fllo convertible child seats because loose foam pieces can pose a choking hazard to children.
Product
CHILD SEAT recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Food)·F-0215-2022·2021-12-01
King's Hawaiian Hamburger Buns recalled for plastic contamination
King's Hawaiian Hawaiian Sweet Hamburger Buns may contain small plastic foreign material. Products on hold for quality inspection were accidentally released into commerce.
Product
Kings Hawaiian Hawaiian Sweet Hamburger Buns8 buns NET WT 12.8 oz. (362.9 g) UPC 0 73435-06050 Product Number 800020
Category
Food
Distribution
5 states
HighFDA (Devices)·Z-0238-2022·2021-12-01
Philips Azurion System Recall for 3D Image Reconstruction Defect
Philips Healthcare is recalling Azurion systems with software releases 2.1(L1) and 2.1(L2) due to a software defect that prevents proper reconstruction of 3D X-ray images when the detector is positioned outside required tolerance.
Product
Philips Azurion systems with software releases 2.1(L1) and 2.1(L2)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0272-2022·2021-12-01
Clinical Chemistry Analyzer Software Defects May Produce Inaccurate Results
Abbott ARCHITECT clinical chemistry analyzers with software 9.41 and earlier contain defects affecting calibration, sample handling, and quality control that may produce inaccurate diagnostic results.
Product
ARCHITECT c4000 REF 02P24-01/2P24, 1P86, 1R24, and 1R25; ARCHITECT c8000 REF 01G06-11/1G06; ARCHITECT c16000 REF 03L77-01/3L77;
Category
Medical Device
Distribution
50 states
HighFDA (Devices)·Z-0273-2022·2021-12-01
Medtronic Cardioblate CryoFlex Ablation Console Recalled for Electrical Connectivity Loss
Medtronic is recalling 7 Cardioblate CryoFlex Surgical Ablation Consoles due to potential intermittent electrical connectivity loss between the console and probe.
Product
Cardioblate CryoFlex Surgical Ablation Console
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0301-2022·2021-12-01
Siemens Artis Q angiography systems may fail to deliver x-ray during procedures
Siemens Artis Q angiography systems may fail to release x-ray when source-to-image distance lift and x-ray release are activated simultaneously, causing procedure delays.
Product
Artis Q ceiling with software VD12-angiography systems developed for single and biplane diagnostic imaging and interventional procedure Model Number: 10848281
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0274-2022·2021-12-01
Freelite Human Lambda Free Kit Recalled for Calibration Curve Inaccuracy
The Binding Site Group recalled 2,254 Freelite Human Lambda Free Kits due to calibration curve issues that may produce higher-than-expected activity readings and affect measurement accuracy.
Product
Freelite Human Lambda Free Kit (for use on the SPAPLUS) REF LK018.S Freelite Human Lambda Free Kit (for use on the SPAPLUS) (x10) REF LK018.10S
Category
Medical Device
Distribution
13 states
HighNHTSA·21V935000·2021-12-01
Audi Recalls 2022 E-Tron GT Vehicles Due to Air Suspension Defect
Volkswagen Group of America is recalling 2022 Audi E-Tron GT vehicles because a loose retaining ring on air suspension struts may compromise handling and increase crash risk.
Product
AUDI — AUDI E-TRON GT
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0295-2022·2021-12-01
Medtronic Wireless Recharger Model WR9200 Becomes Unresponsive on Improper Use
Medtronic is recalling the Wireless Recharger Model WR9200 used with RestoreUltra and RestoreSensor neurostimulator implants. The recharger becomes unresponsive if charging instructions from the user guide are not followed correctly.
Product
Medtronic Wireless Recharger Model WR9200 included in the RS7200 Recharger Kit used by the RestoreUltra (Model 37712), RestoreSensor (Model 37714), Restore Ultra SureScan MRI (Model 97712), and RestoreSensor SureScan MRI (Model 97714) implantable neurostimulators.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0283-2022·2021-12-01
CT Scanner Software Issue May Interrupt Diagnostic Workflows and Delay Diagnoses
Siemens SOMATOM Force CT scanners with software syngo.CT VB20 may experience workflow interruptions, causing diagnosis delays and requiring additional patient scans and contrast media. No illnesses or injuries have been reported.
Product
SOMATOM Force with software syngo.CT VB20 Model #10742326
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·21T018000·2021-11-30
Sailun Recalls Specific Tires Due to Belt Separation Risk
Sailun is recalling specific ST235/80R16 and ST235/85R16 tires due to a manufacturing issue that may cause belt separation. This defect could lead to loss of vehicle control and increase crash risk.
Product
TIRES:TREAD/BELT recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21E097000·2021-11-30
Tenneco Recalls MOOG and NAPA Tie Rods Due to Heat Treatment Defect
Tenneco Automotive is recalling specific MOOG and NAPA tie rods that may not have been heat-treated properly. This defect can cause tie rod failure and loss of steering control.
Product
STEERING:LINKAGES:TIE ROD ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21E098000·2021-11-30
Meritor Recalls 180 Series Drive Pinions Due to Fracture Risk
Meritor is recalling 180 Series Drive Pinions because they may fracture and engage the parking brake without warning, increasing crash risk.
Product
POWER TRAIN:AXLE ASSEMBLY recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V932000·2021-11-29
Honda Recalls 2016-2020 Models for Hood Latch Striker Defect
Honda is recalling specific Passport, Pilot, and Ridgeline vehicles because a damaged hood latch striker may cause the hood to open while driving, obstructing the driver's view.
Product
HONDA — HONDA RIDGELINE, PASSPORT, PILOT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V931000·2021-11-29
Mercedes-Benz Recalls EQS and S-Class Models for Infotainment Distraction
Mercedes-Benz is recalling 2021-2022 EQS and S-Class vehicles because the infotainment system may allow TV and internet use while driving, increasing crash risk.
Product
MERCEDES-BENZ — MERCEDES-BENZ EQS 580, EQS 450, S 500 4MATIC, S 580
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V930000·2021-11-26
Autocar Recalls 2019-2020 Xpeditor Vehicles for Engine Stall Risk
Autocar is recalling 2019-2020 Xpeditor vehicles with aftermarket power take-off systems because the engine may stall, increasing the risk of a crash.
Product
AUTOCAR — AUTOCAR XPEDITOR
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V929000·2021-11-26
Nova Bus Recalls 2021 LFS Buses for Door Software Defect
Nova Bus is recalling 2021 LFS buses because software may cause the rear passenger door to open or close unexpectedly, posing an injury risk.
Product
NOVA BUS — NOVA BUS LFS
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V927000·2021-11-25
Lamborghini Recalls One 2021 Aventador SVJ Roadster for Oil Line Fire Risk
Lamborghini is recalling one 2021 Aventador SVJ Roadster because improperly tightened oil line screws may detach, causing oil to leak onto hot components and increasing fire risk.
Product
LAMBORGHINI — LAMBORGHINI AVENTADOR SVJ
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Food)·F-0189-2022·2021-11-24
HelloFresh Meal Kit Recalled for Salmonella-Contaminated Onions
HelloFresh is recalling meal kits containing onions from ProSource that may be contaminated with Salmonella Oranienburg. The affected product is from Production Week 28 (starting July 7, 2021) and was distributed nationwide.
Product
HelloFresh Meal Kit Product Code 2-7-17-19-21-25-AB from Production Week 28 (production week start date: 07/07/2021)
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0194-2022·2021-11-24
HelloFresh Meal Kits Recalled Due to Salmonella-Contaminated Onions
HelloFresh is recalling meal kits containing onions from ProSource that are associated with a Salmonella Oranienburg outbreak. The affected products were produced during week 33 in 2021.
Product
HelloFresh Meal Kit Product Code 4-6-9-10-11-13-15-20 from Production Week 33 (production week start date: 8/11/2021)
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0197-2022·2021-11-24
HelloFresh Meal Kit Recalled for Salmonella Contamination in Onions
HelloFresh is recalling meal kits with product code 8-15-19-24 from production week 36 (starting September 1, 2021) nationwide because the onions used contain Salmonella Oranienburg.
Product
HelloFresh Meal Kit Product Code 8-15-19-24 from Production Week 36 (production week start date: 09/01/2021)
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0179-2022·2021-11-24
White Onions Recalled Due to Potential Salmonella Contamination
JF Palmer & Sons Produce is recalling white onions packaged in 50-pound bulk bags due to potential Salmonella contamination. The recall affects onions distributed to Minnesota, Texas, California, and Maryland.
Product
Onions White, Medium, Large, Jumbo, packaged in 50 pound bulk bags
Category
Food
Distribution
4 states
SevereFDA (Drugs)·D-0253-2022·2021-11-24
Tinactin Tolnaftate Powder Spray Recalled Due to Benzene Contamination
Bayer Healthcare Pharmaceuticals is recalling Tinactin (Tolnaftate 1%) Powder Spray because some cans contain benzene contamination. Consumers should stop using affected lots and consult a healthcare provider.
Product
Tinactin (Tolnaftate 1%) POWDER SPRAY NET WT 133g (4.6 oz) can, labeled as (a) Product of Ireland 86940418; (b)Product of Finland 20006106; Dist by: Bayer Healthcare LLC, Whippany, NJ 07981, Product of Finland, UPC 3 11017 41009 7, NDC 11523-0777-2.
Category
Drug
Distribution
Distributed nationwide

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