Product Recalls in New Hampshire

Product recalls affecting New Hampshire — including food, drugs, consumer products, medical devices, and vehicles distributed to New Hampshire. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,540 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,540 in last 12 months

Showing 73217340 of 27,899 recalls

Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: Surgical room Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: STRADIS HEALTHCARE Recalled by Stradis Medical, LLC dba Stradis Healthcare...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 2, 2022· Stradis Medical, LLC dba Stradis Healthcare

Recalled Item: HENRY SCHEIN Recalled by Stradis Medical, LLC dba Stradis Healthcare Due to...

The Issue: Medical and surgical procedure trays and kits underwent certain...

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 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"GERALD BIPOLAR FORCEPS INSULATED 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-STYLE 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 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 BAYONET INSULATED IRRIGATING BIPOLAR FORCEPS...

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 JEWELERS BIPOLAR FORCEPS 0.4MM 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 ADSON BIPOLAR FORCEPS 1.0MM TIP OVERALL LENGTH...

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 euro/Spine TITANIUM ROUND HANDLE BAYONET BIPOLAR...

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 TIPS...

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 ROUND HANDLE BAYONET 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 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 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