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. 2,856 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,856 in last 12 months

Showing 2292122940 of 30,923 recalls

Medical DeviceNovember 30, 2015· Bayer Healthcare

Recalled Item: Medrad Source Administration Sets Recalled by Bayer Healthcare Due to The...

The Issue: The firm's investigation of the Medrad Intego indicates that the inner...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Verathon, Inc.

Recalled Item: GlideScope Video Laryngoscope (GVL) Recalled by Verathon, Inc. Due to...

The Issue: Certain models and serial numbers of GlideScope GVL and AVL laryngoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Verathon, Inc.

Recalled Item: GlideScope AVL Video Laryngoscope (AVL) Recalled by Verathon, Inc. Due to...

The Issue: Certain models and serial numbers of GlideScope GVL and AVL laryngoscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Baxter Healthcare Corp.

Recalled Item: Baxter INTERLINK System Recalled by Baxter Healthcare Corp. Due to Potential...

The Issue: Potential for dark loose particulate matter (400 microns or smaller) on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Aesculap, Inc.

Recalled Item: Columbus Revision Knee System Recalled by Aesculap, Inc. Due to Aesculap...

The Issue: Aesculap Inc. US has initiated a recall on Tibial and Femur extension...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 30, 2015· Acumedia Manufacturers, Inc.

Recalled Item: Palcam Supplement Acumedia PN 7987 Product Usage: PALCAM Supplement is...

The Issue: Contamination of product with possible Bacillus spp

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 27, 2015· Leica Microsystems, Inc.

Recalled Item: Bond Polymer Red Detection DS9390 kits. The common name Recalled by Leica...

The Issue: The Firm informed the importer/distributor, Leica Microsystems, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare IntelliVue Info Center iX Recalled by Philips Electronics...

The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare PIIC Classic Upgrade Recalled by Philips Electronics...

The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Philips Electronics North America Corporation

Recalled Item: Philips Healthcare IntelliVue Info Center iX Recalled by Philips Electronics...

The Issue: Reconstructed ECG leads viewed or printed at the Information Center iX may...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Abeon Medical Corporation

Recalled Item: Wilson Penile Implantation System Retractor Frame Recalled by Abeon Medical...

The Issue: The firm was notified by some of their customers that some of the sealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Abeon Medical Corporation

Recalled Item: TLC¿ Self-Retaining Retractor Frames SINGLE USE ONLY Rx ONLY (USA) Recalled...

The Issue: The firm was notified by some of their customers that some of the sealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· RenovoRx, Inc.

Recalled Item: RenovoCath RC 120 Recalled by RenovoRx, Inc. Due to Incorrect version of...

The Issue: Incorrect version of Instructions for Use were shipped to two US customers.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Boston Scientific Corporation

Recalled Item: Boston Scientific ACUITY Pro Coronary Sinus Guide Catheter Recalled by...

The Issue: Potential for separation of the proximal handle from the shaft.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Abeon Medical Corporation

Recalled Item: TLC¿ Self Retaining Retractor System Contents 1-RETRACTOR FRAME 6-ELASTIC...

The Issue: The firm was notified by some of their customers that some of the sealed...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Hex Try-in Screw (5 pk) Dental implants Recalled by Biomet 3i, LLC...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Preformance Post Dental implants Recalled by Biomet 3i, LLC Due to...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Cover Screw Recalled by Biomet 3i, LLC Due to Pouches may not have been...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Certain Provide Abutment Dental implants Recalled by Biomet 3i, LLC Due to...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2015· Biomet 3i, LLC

Recalled Item: Locator Extra Light Angled Replacement Males 4pk Dental implants Recalled by...

The Issue: Pouches may not have been sealed during packing.

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

Class II — Potential Health HazardOngoing