Product Recalls in Alabama

Product recalls affecting Alabama — including food, drugs, consumer products, medical devices, and vehicles distributed to Alabama. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,467 recalls have been distributed to Alabama in the last 12 months.

50,591 total recalls
2,467 in last 12 months

Showing 2698127000 of 28,641 recalls

Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx100 GUIDING CATH S2 Product Code: GSM51000000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx90 GUIDING CATH S2 Product Code: GSM60900000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx100 GUIDING CATH HH Product Code: GHH61000000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx90 GUIDING CATH S2 Product Code: GSM50900000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx100 GUIDING CATH MC Product Code: GCB51000000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx90 GUIDING CATH MPC Product Code: GMC60900000 Intended for...

The Issue: Sterility of device may be compromised due to lack of packaging integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx90 GUIDING CATH ST Product Code: GST50900000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MPD Product Code: GMD60900000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MC Product Code: GCB61000000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx100 GUIDING CATH ST Product Code: GST51000000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Synthes USA HQ, Inc.

Recalled Item: Synthes Dens Instrument Set (Dens Graphic Case) Recalled by Synthes USA HQ,...

The Issue: The Dens Instrument Set has been designed to facilitate the anterior...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx100 GUIDING CATH HH Product Code: GMC51000000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx90 GUIDING CATH MPD Product Code: GMD50900000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx100 GUIDING CATH S2 Product Code: GSM61000000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx100 GUIDING CATH ST Product Code: GST61000000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMD61000000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx90 GUIDING CATH ST Product Code: GST60900000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx90 GUIDING CATH HH Product Code: GHH60900000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Synthes USA HQ, Inc.

Recalled Item: Flexible Grip which is part of the Synthes Universal Nail Recalled by...

The Issue: Synthes is initiating a voluntary recall of the Flexible Grip (Part number...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 5Fx90 GUIDING CATH MPC Product Code: GMC50900000 Intended for...

The Issue: Sterility of device may be compromised due to lack of package integrity

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

Class II — Potential Health HazardOngoing