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. 2,367 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,367 in last 12 months

Showing 2786127880 of 27,899 recalls

Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 50mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 55mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 35mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 45mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 50mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 5.5mm x 45mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 40mm Noncannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 7.5mm x 30mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2009· NuVasive Inc

Recalled Item: 6.5mm x 40mm Cannulated Screw Shank Subsequent Codes: KWP Recalled by...

The Issue: The tulip portion of the screw assembly can disengage from the shank after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 10, 2008· GE OEC Medical Systems, Inc

Recalled Item: GEHC OEC Injection Cable for MedRad Provis V Contrast Injector. Recalled by...

The Issue: GE initiated a correction to the instructions/use due to the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2008· Sechrist Industries Inc

Recalled Item: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model...

The Issue: Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 28, 2008· Sechrist Industries Inc

Recalled Item: Sechrist Monoplace Hyperbaric Chamber with Electronic Control Module Model...

The Issue: Sechrist conducted a field upgrade on the hyperbaulic chambers equipped with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2008· SRI Surgical

Recalled Item: Various SRI Surgical Disposable Accessory Packs. SRI's Disposable Accessory...

The Issue: Distribution of a product that did not meet specifications. (labeling error)

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 12, 2008· Ventana Medical Systems Inc

Recalled Item: Benchmark XT/LT and Discovery XT Model Numbers: N750-BMK-FS Recalled by...

The Issue: Ventana Medical System is initiating the recall of the BenchMark and...

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

Class II — Potential Health HazardOngoing