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. 2,409 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,409 in last 12 months

Showing 1894118960 of 27,899 recalls

Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS 4F Stiffened Micro-Introducer Recalled by Angiodynamics, Inc....

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Zimmer Biomet, Inc.

Recalled Item: Zimmer¿ Gender Solutions" Patellofemoral Joint Prosthesis Milling Handpiece...

The Issue: Complaints have been reported that the handpiece is inoperable. The...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 4...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: Baxter SIGMA Spectrum INFUSION PUMP with Master Drug Library Recalled by...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: sigma spectrum VOLUMETRIC INFUSION PUMP with Master Drug Library Recalled by...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Baxter Healthcare Corp.

Recalled Item: V6 Rear Case Assembly Recalled by Baxter Healthcare Corp. Due to A...

The Issue: A correction was issued for the SIGMA Spectrum Infusion Pump with Master...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 28, 2016· Angiodynamics, Inc.

Recalled Item: ANGIODYNAMICS Percutaneous Introducer Set under the following labels: 1) 5...

The Issue: Greatbatch Medical the manufacturer of the 4F and 5F sheath/dilator...

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

Class III — Low RiskOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRIPLE PRESSURE KIT W/03ML FLUSH DEVICE FOR UNIV. OF IOWA Recalled by ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Transpac¿ IV Monitoring Kit w/Arterial 84" Safeset" Reservoir Recalled by...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: CATH LAB KIT WITH 03ML FLUSH DEVICE FOR CARLE CLINIC Recalled by ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRANSPAC¿ IV MONITORING KIT WITH DISPOSABLE TRANSDUCER Recalled by ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Transpac¿ w/Safeset Reservoir Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: TRANSPAC¿ IV DISPOSABLE TRANSDUCER WITH STOPCOCKS Recalled by ICU Medical,...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Cath Lab Kit For Elkhart Hosp. Recalled by ICU Medical, Inc. Due to ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: PERFUSION KIT W/03ML FLUSH DEVICE FOR NE REGIONAL MED. CTR Recalled by ICU...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 27, 2016· ICU Medical, Inc.

Recalled Item: Transpac¿ IV Monitoring Kit Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical Inc. has identified a potential for leak with certain SafeSet...

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

Class II — Potential Health HazardOngoing