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

10601–10625 of 13748

HighFDA (Devices)·Z-0357-2023·2022-12-14
Dover Urethral Catheter Drainage System Recall for Potential Port Blockage
Cardinal Health is recalling Dover closed urethral catheter trays because the drainage bag port may become occluded, preventing urine from draining properly and increasing the risk of urinary retention.
Product
Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter 16 Fr/Ch (5.3 mm) Product Code: 3408 Intended for urinary drainage from the bladder of a patient
Category
Medical Device
Distribution
Distributed nationwide
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-0355-2023·2022-12-14
Siemens IMMULITE Testosterone Assay Recalled for Measurement Bias
Siemens is recalling two lots of its IMMULITE Total Testosterone Assay due to a confirmed 40% positive measurement bias at higher testosterone levels, which may delay diagnosis and require repeat testing.
Product
IMMULITE and IMMULITE 1000 Total Testosterone Assay- In vitro diagnostic use with the IMMULITE and IMMULITE 1000 Analyzers for the quantitative measurement of total testosterone in serum and heparinized plasma.
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-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-0361-2023·2022-12-14
Dover Urinary Catheter Drainage Bag Port Occlusion Recall
Cardinal Health is recalling Dover closed urethral catheter trays due to potential occlusion of the drainage bag inlet port, which may prevent proper 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: 3450LF Intended for urinary drainage from the bladder of a patient.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0463-2023·2022-12-14
Philips MR 7700 System Upgrade Recalled Due to Gradient Coil Fire Risk
Philips is recalling the Upgrade to MR 7700 System (Model 782130) because the gradient coil may act as a heat source and produce smoke or fire. Affected units should not be operated until Philips provides further guidance.
Product
Philips Upgrade to MR 7700 System, Model Number 782130
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0425-2023·2022-12-14
FAST Sample Preparation System Labeling Corrected for Regulatory Scope
Qvella is correcting documentation for the FAST System, a blood culture sample preparation device, because it exceeded its original regulatory scope. The company is updating manuals and promotional materials to clarify approved applications.
Product
The FAST System and the FAST PBC Prep Cartridge together are a closed, rapid and automated sample preparation system for isolating bacterial cells directly from a positive blood culture (PBC). The cartridge and instrument isolate and concentrate bacterial cells directly from PBC
Category
Medical Device
Distribution
4 states
ModerateFDA (Devices)·Z-0383-2023·2022-12-14
Bipolar Forceps Recall Due to Incomplete Instructions for Use
Carefusion is recalling 259 surgical bipolar forceps units because the Instructions for Use are missing critical information about power supply interface and maintenance procedures.
Product
Carefusion V. Mueller GERALD BAYONET BIPOLAR FORCEPS 1.0MM TIP, INSULATED OVERALL LENGTH 7-1/2" (190MM), REF F-1113
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0464-2023·2022-12-14
Port Access Kits incorrectly labeled as IV Start Kits
Medical Action Industries is recalling Port Access Kits that are incorrectly labeled as IV Start Kits on the individual kit label. The case label is correct; mislabeling could cause confusion about the product's identity.
Product
Medical Action Industries Inc. Port Access Kit, REF #76511B (on case label), sterile; and Medical Action Industries Inc. IV Start Kit, REF #78019 (on kit label), sterile. Kit components are the Port Access Kit.
Category
Medical Device
Distribution
1 state
ModerateFDA (Devices)·Z-0389-2023·2022-12-14
Carefusion Bipolar Surgical Forceps Recalled for Missing Instructions
Carefusion 2200 Inc. is recalling 41 units of Hardy Bayonet Irrigating Bipolar Forceps due to incomplete instructions for use. The supplied instructions lack content about device power supply interface and maintenance procedures.
Product
Carefusion V. Mueller HARDY BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED, 0.5MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-1335
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0379-2023·2022-12-14
Bipolar Forceps Recall: Missing Device Instructions for Use
Carefusion is recalling bipolar forceps due to missing instructions for use. The corrected instructions address power supply interface, cleaning, and maintenance.
Product
Carefusion V. Mueller SEMKIN BIPOLAR FORCEPS 1.5MM TIP, INSULATED OVERALL LENGTH 6" (150MM), REF F-1045
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0412-2023·2022-12-14
Bipolar Surgical Forceps Recalled for Missing Instruction Manual Content
CareFusion bipolar forceps recalled due to missing instructions on power supply interface and cleaning/maintenance procedures. Corrected documentation is now available.
Product
CareFusion V. Mueller Neuro/Spine TITANUIM BIPOLAR FORCEPS STRAIGHT, 0.25MM TIP OVERALL LENGTH 6" (150MM) , REF F-5128
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0411-2023·2022-12-14
Bipolar Forceps Recall: Missing Power Supply and Cleaning Instructions
Carefusion is recalling bipolar forceps due to incomplete Instructions for Use. The IFU is missing content about power supply interface and cleaning procedures.
Product
CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS, 0.5MM TIP, ANGLED-UP FINE OVERALL LENGTH 8-3/4" (225MM), REF F-5127
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0396-2023·2022-12-14
CareFusion Bipolar Forceps Recalled for Incomplete Instructions for Use
CareFusion bipolar forceps are recalled due to incomplete manufacturer instructions for use. Missing content covers power supply interface and device maintenance and cleaning procedures.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 8-1/2" (215MM), REF F-5002
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0406-2023·2022-12-14
Bipolar Forceps Recall: Missing Instructions for Power Supply and Maintenance
CareFusion bipolar forceps are being recalled due to missing Instructions for Use content about power supply interface, cleaning, and maintenance. Users should obtain the complete manufacturer instructions immediately.
Product
CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS, 1.0MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5069
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0398-2023·2022-12-14
CareFusion Bipolar Surgical Forceps Recalled by FDA Class II Voluntary Action
CareFusion initiated a voluntary recall of bipolar forceps surgical instruments. The recall affects 4 units distributed nationwide and internationally.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS, 0.7MM TIP OVERALL LENGTH 9-1/2" (240MM) , REF F-5008
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0403-2023·2022-12-14
CareFusion Bipolar Forceps Recalled: Incomplete Instructions for Power Supply
CareFusion is recalling bipolar forceps units due to incomplete instructions for power supply interface and device maintenance. The recall affects devices distributed worldwide.
Product
CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM TIP OVERALL LENGTH 10-1/2" (265MM), REF F-5022
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0424-2023·2022-12-14
HF Resection Electrodes Recalled for Incompatible Packaged Cable
Olympus Corporation is recalling HF Resection Electrodes because an incompatible cable may be included in packaging. The cable cannot connect to the electrosurgical generator, potentially delaying or canceling surgery.
Product
HF Resection Electrodes, Model Numbers WA22602S, WA22603S, WA22621S and WA22657S
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0414-2023·2022-12-14
CareFusion Bipolar Surgical Forceps Recalled for Incomplete Instructions
CareFusion bipolar surgical forceps are being recalled because their instruction manual is missing critical information about power supply interface and cleaning procedures. BD is providing corrected instructions to healthcare facilities.
Product
CareFusion V. Mueller TITANIUM BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED STRAIGHT FINE, 0.5MM TIP OVERALL LENGTH 8-3/4" (225MM), REF F-5302
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0404-2023·2022-12-14
Bipolar Forceps Device Incomplete Instructions for Use Recalled
CareFusion bipolar forceps (REF F-5061) recalled due to incomplete Instructions for Use missing device power supply interface and cleaning instruction content.
Product
CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.0MM TIP OVERALL LENGTH 9-1/2" (240MM), REF F-5061
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0388-2023·2022-12-14
Bipolar Irrigating Forceps Recall: Missing Power Supply and Maintenance Instructions
Carefusion is recalling 132 units of V. Mueller bipolar irrigation forceps due to incomplete instruction manuals missing power supply interface and maintenance guidance.
Product
Carefusion V. Mueller SCOVILLE-GREENWOOD BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED, 1.5MM TIP OVERALL LENGTH 7-3/4" (195MM), REF F-1305
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0386-2023·2022-12-14
Bipolar Surgical Forceps Recalled for Incomplete Instructions for Use
Carefusion bipolar surgical forceps recalled nationwide due to incomplete Instructions for Use. The distributed IFU is missing guidance on power supply interface and cleaning and maintenance procedures.
Product
Carefusion V. Mueller GERALD BAYONET BIPOLAR FORCEPS 1.0MM TIP, INSULATED IRRIGATING OVERALL LENGTH 7-1/2" (190MM), REF F-1303
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0384-2023·2022-12-14
Bipolar Forceps Recall: Missing Device Power Supply and Maintenance Instructions
Carefusion recalls bipolar forceps due to incomplete Instructions for Use missing power supply interface and maintenance guidance. No injuries reported.
Product
Carefusion V. Mueller CUSHING BAYONET BIPOLAR FORCEPS, 0.7MM TIP, INSULATED IRRIGATING OVERALL LENGTH 7-1/2" (190MM), REF F-1300
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0392-2023·2022-12-14
Carefusion Bipolar Forceps Recalled for Incomplete Instructions for Use
Carefusion is recalling the V. Mueller Jewelers Bipolar Forceps due to incomplete Instructions for Use missing power supply interface and cleaning/maintenance instructions. The recall affects 236 units distributed nationwide and internationally.
Product
Carefusion V. Mueller JEWELERS BIPOLAR FORCEPS 0.4MM TIP, STRAIGHT OVERALL LENGTH 4" (100MM), REF F-3000
Category
Medical Device
Distribution
Distributed nationwide

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10601–10625 of 13748