Product Recalls in California

Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,774 recalls have been distributed to California in the last 12 months.

56,506 total recalls
1,774 in last 12 months

Showing 77817800 of 30,923 recalls

Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS Recalled...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: Carefusion V. Mueller GERALD BAYONET BIPOLAR FORCEPS 1.0MM TIP Recalled by...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller CUSHING BAYONET BIPOLAR INSULATED FORCEPS Recalled by...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: Carefusion V. Mueller" SCOVILLE-GREENWOOD BAYONET BIPOLAR FORCEPS 1.5MM TIP...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: Carefusion V. Mueller JEWELERS BIPOLAR FORCEPS 0.4MM TIP Recalled by...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: Carefusion V. Mueller HARDY BAYONET BIPOLAR FORCEPS WITH STOP Recalled by...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 1.5MM...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: Carefusion V. Mueller GERALD BAYONET IRRIGATING BIPOLAR FORCEPS 1.0MM TIP...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS 0.7MM...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller TITANIUM BAYONET BIPOLAR FORCEPS Recalled by...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller Neuro/Spine TITANIUM BAYONET INSULATED IRRIGATING...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller TITANIUM BAYONET IRRIGATING BIPOLAR FORCEPS INSULATED...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller Neuro/Spine TITANUIM BIPOLAR FORCEPS STRAIGHT Recalled...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Bunnell, Inc.

Recalled Item: 2.5 mm LifePort Endotracheal Tube Adapters 10-pack Recalled by Bunnell, Inc....

The Issue: Some adaptors, for use with high frequency ventilators, were packaged...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller ROUND HANDLE BAYONET BIPOLAR FORCEPS Recalled by...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Carefusion 2200 Inc

Recalled Item: CareFusion V. Mueller TITANIUM ROUND HANDLE BAYONET BIPOLAR FORCEPS Recalled...

The Issue: BD has determined that the Instructions For Use (IFU) provided by BD is...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Qvella Corporation

Recalled Item: The FAST System and the FAST PBC Prep Cartridge together are a closed...

The Issue: Device exceeds the limitations of a Class I 510(k)-exempt device so the user...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2022· Cardinal Health

Recalled Item: Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter Recalled...

The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2022· Randox Laboratories Ltd.

Recalled Item: IgA Immunoturbidimetric Assay- In vitro determination of IgA and IgM...

The Issue: Update to the carryover avoidance technical bulletin to detail that IgA and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2022· Cardinal Health

Recalled Item: Dover Closed Urethral Tray with Hydrogel Coated Red Rubber Catheter Recalled...

The Issue: Occlusion (blockage) of the bubble inlet port of the urinary drainage bag...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing