Product Recalls in Michigan

Product recalls affecting Michigan — including food, drugs, consumer products, medical devices, and vehicles distributed to Michigan. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,520 recalls have been distributed to Michigan in the last 12 months.

53,342 total recalls
2,520 in last 12 months

Showing 2764127660 of 29,286 recalls

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· Codman & Shurtleff, Inc.

Recalled Item: NEUROPATH 6Fx90 GUIDING CATH MCV Product Code: GCB60900000 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 HH Product Code: GHH51000000 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 5Fx100 GUIDING CATH MP Product Code:GMD51000000 Intended for use...

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: GMC61000000 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 MCV Product Code: GCB50900000 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 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
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· 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 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 HH Product Code: GHH50900000 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 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 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 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 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