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 82018220 of 27,899 recalls

Medical DeviceMarch 9, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Medline Standard PVC Laryngeal Masks Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: The mask cuff may disconnect from the device's breathing tube.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2022· Olympus Corporation of the Americas

Recalled Item: BF-MP60: OES Bronchofiberscope Recalled by Olympus Corporation of the...

The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2022· Olympus Corporation of the Americas

Recalled Item: BF-3C160: EVIS EXERA Bronchovideoscope Recalled by Olympus Corporation of...

The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2022· Olympus Corporation of the Americas

Recalled Item: BF-MP160F: EVIS EXERA Bronchofibervideoscope Recalled by Olympus Corporation...

The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2022· Olympus Corporation of the Americas

Recalled Item: BF-1TQ180: EVIS EXERA II Bronchovideoscope Recalled by Olympus Corporation...

The Issue: Bronchofiberscope Updated instructions on the use of certain chemicals to be...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2022· SIMPLIVIA HEALTHCARE LTD.

Recalled Item: OnGuard2 CSTD Bag Adaptor SP A Chemfort CSTD Product Recalled by SIMPLIVIA...

The Issue: Disconnection of the OnGuard2 Bag Adaptor SP from infusion bags which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 8, 2022· Abbott Laboratories

Recalled Item: ARCHITECT STAT Myoglobin Calibrators Recalled by Abbott Laboratories Due to...

The Issue: This calibrator lot did not meet acceptance criteria during ongoing...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc.

Recalled Item: Acuson 9vE4 Transducer Recalled by Siemens Medical Solutions USA, Inc. Due...

The Issue: Transducers (component of ultrasound system) may exceed recommended thermal...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...

The Issue: Upgraded software version makes an automatic change in laser configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on syngo.via Recalled by...

The Issue: Upgraded software version makes an automatic change in laser configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...

The Issue: Upgraded software version makes an automatic change in laser configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: syngo.via RT Image Suite upgraded to VB60 running on SOMATOM Recalled by...

The Issue: Upgraded software version makes an automatic change in laser configuration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS SOMATOM with software syngo CT VA30A_SP4 Models: SOMATOM go.Now...

The Issue: Software error may result in sporadic problems causing scanning workflow...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 7, 2022· Siemens Medical Solutions USA, Inc

Recalled Item: YSIO X.Pree Recalled by Siemens Medical Solutions USA, Inc Due to For the...

The Issue: For the automated multi-image-acquisition procedure Ortho x-ray collimation...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2022· SML Distribution, LLC

Recalled Item: Skippack Medical Lab SARS-CoV-2 Antigen Rapid Test Kit (Colloidal Gold)...

The Issue: The product was distributed without FDA authorization or clearance for...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 4, 2022· Draegar Medical Systems, Inc.

Recalled Item: Drager Infinity CentralStation Software versions VG2.1.2 and VG2.1.2 SU12....

The Issue: Software issue resulting in temporary loss of central monitoring functionality.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2022· GE Healthcare, LLC

Recalled Item: GE Healthcare MR Systems Recalled by GE Healthcare, LLC Due to During the...

The Issue: During the de-installation of an MR system magnet, if all rigging and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2022· Abbott Molecular, Inc.

Recalled Item: Alinity m HBV AMP Kit (US and CE) Recalled by Abbott Molecular, Inc. Due to...

The Issue: There is a potential for misquantitation high results for negative samples.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2022· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: Excelsior Medical 10mL Sterile Field Saline Flush ZR Recalled by MEDLINE...

The Issue: Sterility failure of the exterior of the syringe which may impact the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2022· Abbott Molecular, Inc.

Recalled Item: Alinity m HBV Application Specification File (US and CE) Recalled by Abbott...

The Issue: There is a potential for misquantitation high results of negative samples.

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

Class II — Potential Health HazardOngoing