Product Recalls in California

Product recalls affecting California — including food, drugs, consumer products, medical devices, and vehicles distributed to California. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,839 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,839 in last 12 months

Showing 2916129180 of 30,923 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 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 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· Acclarent, Inc.

Recalled Item: Inspira AIR Balloon Dilation system. Size 7 x 24 mm Recalled by Acclarent,...

The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...

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 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· Synthes USA HQ, Inc.

Recalled Item: Synthes Multi-Vector Distractor Body Recalled by Synthes USA HQ, Inc. Due to...

The Issue: It was discovered that the sheer pin on the Multi-Vector Distractor may not...

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· Acclarent, Inc.

Recalled Item: Inspira AIR Balloon Dilation system. Size 14 x 40 mm Recalled by Acclarent,...

The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...

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 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 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 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· Acclarent, Inc.

Recalled Item: Inspira AIR Balloon Dilation system. Size 5 x 24 mm Recalled by Acclarent,...

The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...

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· Synthes USA HQ, Inc.

Recalled Item: Synthes Spine 5.2mm Titanium Click ' X Pedicle Screw Dual Recalled by...

The Issue: Lot number 7542279, of the 45 mm Click 'X Pedicle Screw (Part number...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 11, 2013· Acclarent, Inc.

Recalled Item: Inspira AIR Balloon Dilation system. Size 10 x 40 mm Recalled by Acclarent,...

The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...

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