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 deaths or serious injuries are reported, 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

9051–9075 of 27441

HighFDA (Devices)·Z-0407-2023·2022-12-14
Bipolar Forceps Recalled for Missing Instructions on Cleaning and Power Supply
CareFusion V. Mueller bipolar forceps (Ref F-5073) recalled due to missing critical instructions for power supply interface and cleaning and maintenance procedures. Users should obtain the complete Instructions For Use from the manufacturer.
Product
CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5073
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0394-2023·2022-12-14
Surgical Bipolar Forceps Recalled for Missing Safety Instructions
Carefusion is recalling surgical bipolar forceps due to incomplete instructions for use. The missing information covers power supply interface and cleaning and maintenance procedures.
Product
Carefusion V. Mueller ADSON BIPOLAR FORCEPS 1.0MM TIP OVERALL LENGTH 4-3/4" (120MM), REF F-3010
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0397-2023·2022-12-14
Bipolar Surgical Forceps Recalled for Incomplete Instructions for Use
CareFusion bipolar surgical forceps recalled due to incomplete Instructions for Use missing power supply interface and maintenance guidance.
Product
CareFusion V. Mueller euro/Spine TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-5006
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0368-2023·2022-12-14
Treadmill safety mechanism may fail to stop during fall
Full Vision Inc. Trackmaster treadmills (Model #317-07926GE) may fail to stop during a fall if the magnetic safety mechanism malfunctions. 69 units are affected.
Product
FULL VISION INC. TRACKMASTER, TREADMILL GE T2100-ST1 110V, Model #317-07926GE
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0393-2023·2022-12-14
Bipolar forceps recall for incomplete operating and maintenance instructions
Carefusion is recalling neurosurgical bipolar forceps due to incomplete Instructions for Use. The product is missing critical information about power supply interface and cleaning/maintenance procedures.
Product
Carefusion V. Mueller Neuro/Spine JEWELERS BIPOLAR FORCEPS 0.4MM TIP, CURVED, # 7 OVERALL LENGTH 4-3/4" (120MM), REF F-3007
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0395-2023·2022-12-14
CareFusion Bipolar Forceps Recalled for Incomplete Instructions for Use
CareFusion 2200 Inc is recalling 4,557 units of V. Mueller ADSON Bipolar Forceps due to incomplete Instructions for Use. The IFU is missing content about power supply interface and cleaning and maintenance instructions.
Product
CareFusion V. Mueller ADSON BIPOLAR FORCEPS 1.0MM TIP, INSULATED OVERALL LENGTH 4-3/4" (120MM), REF F-3015
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0382-2023·2022-12-14
Surgical Bipolar Forceps Recalled for Missing Instructions
Carefusion is recalling the V. Mueller Bipolar Forceps Insulated due to missing instructions for power supply interface and cleaning/maintenance procedures.
Product
Carefusion V. Mueller"GERALD BIPOLAR FORCEPS INSULATED, 1.0MM TIP OVERALL LENGTH 7" (180MM), REF F-1112
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0460-2023·2022-12-14
Philips Ingenia Elition X MR System Gradient Coil Fire and Smoke Hazard
Philips is recalling 566 Ingenia Elition X MRI systems nationwide. The gradient coil may act as a heat source with the potential to produce smoke and/or fire.
Product
Philips Ingenia Elition X MR System, Model Numbers 781358, 782107, 782119, 782136
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0365-2023·2022-12-14
Full Vision TrackMaster Treadmill Emergency Stop Failure Recall
Full Vision Inc. is recalling 38 TrackMaster TMX428 220V treadmills due to a rare circuit failure that may prevent the magnetic safety tether from stopping the machine during a fall.
Product
FULL VISION INC. TRACKMASTER,TREADMILL TMX428 220V, Model #317-07927
Category
Medical Device
Distribution
3 states
HighFDA (Devices)·Z-0419-2023·2022-12-14
LineSider Spinal System Screws Recalled for Potential Weld Separation
Integrity Implants is recalling 1,702 LineSider Spinal System pedicle screws due to potential weld separation between screw head components that could result in device failure.
Product
LineSider Spinal System 5.5/6.0mm, Non-mod Standard 7.1mm - Dual Lead, Cannulated. Thoracolumbosacral pedicle screw system; Spinal interlaminal fixation orthosis. Product sold as non-sterile and shipped in protective sterilization trays. Screws can also be shipped individually
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0401-2023·2022-12-14
Bipolar Forceps Recall: Missing Device Use and Maintenance Instructions
CareFusion bipolar forceps recalled due to incomplete Instructions for Use. Missing documentation covers power supply interface and cleaning/maintenance procedures.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 0.7MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5016
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0385-2023·2022-12-14
Surgical Bipolar Forceps Recalled Due to Incomplete Instructions for Use
Carefusion recalls V. Mueller bipolar forceps with incomplete instructions. The device lacks critical information on power supply interface and cleaning procedures.
Product
Carefusion V. Mueller GERALD BAYONET IRRIGATING BIPOLAR FORCEPS 1.0MM TIP OVERALL LENGTH 7-1/2" (190MM), REF F-1301
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0415-2023·2022-12-14
CareFusion Bipolar Forceps Recalled Due to Incomplete Instructions
CareFusion recalls 142 units of bipolar surgical forceps due to incomplete Instructions for Use lacking power supply interface and maintenance guidance found in the manufacturer's version.
Product
CareFusion V. Mueller TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS 1.0MM TIP, STR, MED, INSULATED OVERALL LENGTH 8-3/4" (225MM), REF F-5303
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0416-2023·2022-12-14
Bipolar Surgical Forceps Recalled Due to Missing Instructions for Use
CareFusion 2200 Inc is recalling V. Mueller bipolar forceps (model F-5304) due to missing Instructions for Use content related to power supply interface and cleaning/maintenance procedures.
Product
CareFusion V. Mueller Neuro/Spine TITANIUM BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS 0.5MM TIP, ANGLED-UP, FINE OVERALL LENGTH 8-3/4" (225MM), REF F-5304
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0371-2023·2022-12-14
2.5 mm LifePort Endotracheal Tube Adapters Deformation Risk
Bunnell's 2.5 mm LifePort Endotracheal Tube Adapters may deform due to improper packaging, potentially affecting ventilator performance. The defect may lead to hypercarbia, hypoxia, and gas trapping.
Product
2.5 mm LifePort Endotracheal Tube Adapters 10-pack, Catalog: 9025; and 2.5 mm LifePort Endotracheal Tube Adaptors inside Patient Circuit Kits, Catalog: 938
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0461-2023·2022-12-14
Philips MRI System Recall Due to Fire and Smoke Risk
Philips SmartPath to Ingenia Elition X MR System models may produce smoke or fire due to gradient coil heat. Recall affects 566 units nationwide.
Product
Philips SmartPath to Ingenia Elition X MR System, Model Numbers 782118, 782132, 782144
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0363-2023·2022-12-14
IgM and IgA Assay Kits Recalled for Test Carryover Risk
Randox Laboratories recalls IgM and IgA immunoturbidimetric assay kits due to carryover contamination that can cause elevated test results when run immediately after Fructosamine tests on RX instruments.
Product
IgM Immunoturbidimetric Assay-In vitro determination of IgA and IgM in serum and plasma Catalog Number: IM3834
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0458-2023·2022-12-14
Propel Mini Sinus Implant Recalled for Incorrect Product Label Information
Intersect ENT is recalling 611 units of Propel Mini Mometasone Furoate Sinus Implant due to incorrect product identification information on the label. The label displays wrong reference numbers and UDI-DI codes.
Product
Propel Mini Mometasone Furoate Sinus Implant, with Straight Delivery System, REF 60044
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0387-2023·2022-12-14
Bipolar Forceps Recall Due to Incomplete Instructions for Use
BD recalled Carefusion bipolar forceps due to missing Instructions for Use content regarding power supply interface and cleaning/maintenance. Affected units distributed nationwide and internationally.
Product
Carefusion V. Mueller SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS 1.5MM TIPS, IRRIGATING OVERALL LENGTH 7-3/4" (19.7CM), REF F-1304
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0410-2023·2022-12-14
CareFusion Bipolar Forceps Recalled Due to Missing Instructions for Use
CareFusion V. Mueller bipolar forceps are being recalled because the provided Instructions for Use are missing critical content about power supply interface and cleaning/maintenance. The complete information is available in the manufacturer's full IFU.
Product
CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, 1.0MM TIP, STRAIGHT MEDIUM OVERALL LENGTH 8-3/4" (225MM), REF F-5126
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0374-2023·2022-12-14
Bipolar Surgical Forceps Recalled for Incomplete Instructions for Use
Carefusion is recalling 418 units of bipolar surgical forceps because the provided instructions lack critical content about power supply interface and maintenance. Complete manufacturer instructions are necessary for safe device operation.
Product
CareFusion V. Mueller SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 7-3/4" (195MM) , REF F-1002
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0408-2023·2022-12-14
Bipolar Forceps Recalled for Incomplete Instructions for Use
CareFusion bipolar forceps recalled nationwide due to incomplete Instructions for Use missing power supply interface and cleaning information. The missing content could affect proper device operation and maintenance.
Product
CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, 1.5MM TIP, STRAIGHT STANDARD, 8-3/4" (225MM), REF F-5124
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0409-2023·2022-12-14
Bipolar Forceps Recall Due to Incomplete Instructions for Use
BD is recalling CareFusion bipolar forceps due to incomplete Instructions for Use. The IFU is missing critical information about power supply interface and cleaning/maintenance procedures.
Product
CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, STRAIGHT, FINE 0.5MM TIP OVERALL LENGTH 8-3/4" (225MM), REF F-5125
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0462-2023·2022-12-14
Philips MR 7700 System Recalled for Gradient Coil Fire Risk
Philips is recalling 566 MR 7700 MRI systems nationwide. The gradient coil in these systems may overheat and produce fire or smoke.
Product
Philips MR 7700 System, Model Number 782120
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0360-2023·2022-12-14
Dover urinary catheter drainage bag occlusion defect nationwide recall
Cardinal Health is recalling Dover urinary catheter trays due to potential blockage of the drainage bag inlet port, which may prevent urine drainage and increase the risk of urinary retention.
Product
Dover Closed Urethral Tray with Vinyl Catheter 14 Fr/Ch (4.7 mm), 5 mL Catheter Pre-connected to 1000 mL Drainage Bag Product Code: 3450 Intended for urinary drainage from the bladder of a patient
Category
Medical Device
Distribution
Distributed nationwide

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9051–9075 of 27441