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 2552125540 of 27,899 recalls

Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 90595204117 Articular Surface XLPE CR ART SURF AE56/STGRN 17 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597202009 Articular Surface CR ART SURF 12/PURPLE 09 Recalled by Zimmer,...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597201303 Femur CR POR FM COMP SIZE CML Rx Recalled by Zimmer, Inc. Due to...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597601201 Femur CRA PRECOAT FEM COMP SIZE B/L Rx Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Baxter Healthcare Corp.

Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...

The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597602010 Articular Surface AC ART SURF 12/PUR 10 Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597502010 Provisional AC ART SURF PROV 12/PUR 10 Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597102010 Provisional CR ART SURF PROV 12/PURPLE 10 Recalled by Zimmer,...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00598706201 Provisional CRA FEM PROV/CUT GDE SZ BML Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Codman & Shurtleff, Inc.

Recalled Item: MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc....

The Issue: Miscalibrated Fill Level Sensor may affect dosing level

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597201131 Femur CR POR SURF HDN FEM CO-NID AML Rx Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597603110 Articular Surface AC ART SURF 34/STRIPED YEL 10 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597106126 Provisional MIC POROUS PAT PROV 26MMX10MM Recalled by Zimmer,...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 65597201101 Femur CR POR FEM HATCP SIZE AML Rx Recalled by Zimmer, Inc. Due...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 90595202017 Articular Surface XLPE CR ART SURF AE12/PUR 17 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597101101 Provisional CR PROV FRM COMP SIZE AML Recalled by Zimmer, Inc....

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597001101 Femur CR PRECOAT FEM COMP SIZE AML Recalled by Zimmer, Inc. Due...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597204109 Articular Surface CR ART SURF 56/STRIPE GRN 9 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 00597203109 Articular Surface CR ART SURF 34/STRIPE YEL 09 Recalled by...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2013· Zimmer, Inc.

Recalled Item: 65595201201 Femur CR-FLEX POR HATCP FEM B-L Rx Recalled by Zimmer, Inc. Due...

The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...

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

Class II — Potential Health HazardOngoing