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. 2,836 recalls have been distributed to California in the last 12 months.

56,506 total recalls
2,836 in last 12 months

Showing 3098131000 of 56,506 recalls

Medical DeviceAugust 28, 2017· Zimmer Biomet, Inc.

Recalled Item: Persona Partial Knee System Product Usage: The Persona Partial Knee Recalled...

The Issue: Potential for the Persona Partial Knee Impactor Pad to fracture.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2017· Zimmer Biomet, Inc.

Recalled Item: G7 DUAL MOBILITY LINER 44MM F Product Usage: Intended for Recalled by Zimmer...

The Issue: The affected products are labeled and etched as F-44 mm liners; however, the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2017· Zimmer Biomet, Inc.

Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...

The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 25, 2017· Zimmer Biomet, Inc.

Recalled Item: AGC 2000 LP Patella Recalled by Zimmer Biomet, Inc. Due to The affected AGC...

The Issue: The affected AGC 2000 LP Patella products were over-molded leaving the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2017· Beckman Coulter Inc.

Recalled Item: Lyophilized Chemistry Calibrator Level 1 Product Usage: Beckman Coulter...

The Issue: Unpaired lots of AU lyophilized chemistry calibrator level 1 and 2 have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 24, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: AArtis Q/ Q.Zen biplane Artis zee biplane Product Usage: Artis Recalled by...

The Issue: Within a specific number of Artis zee biplane and Artis Q biplane systems, a...

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

Class II — Potential Health HazardOngoing
FoodAugust 24, 2017· House of Spices India, Inc.

Recalled Item: Laxmi Rusks Recalled by House of Spices India, Inc. Due to Undeclared Soy

The Issue: Product may contain undeclared soy.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2017· Inopak Ltd

Recalled Item: Choice Antibacterial Hand Soap Recalled by Inopak Ltd Due to GMP Deviations;...

The Issue: GMP Deviations; potential bacterial contamination may have been introduced...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2017· Inopak Ltd

Recalled Item: Mild Healthcare Antibacterial Hand Soap Recalled by Inopak Ltd Due to GMP...

The Issue: GMP Deviations; potential bacterial contamination may have been introduced...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 23, 2017· Inopak Ltd

Recalled Item: Option Systems Antibacterial Foaming Hand Wash Recalled by Inopak Ltd Due to...

The Issue: GMP Deviations; potential bacterial contamination may have been introduced...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 23, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.plaza systems with SW VB20A Recalled by Siemens Medical Solutions USA,...

The Issue: When a prior study is being replaced in the workflow step, in certain...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2017· The Binding Site Group, Ltd.

Recalled Item: Human Alpha-1-Antitrypsin Kit for use on the SPAPlus analyser Recalled by...

The Issue: The high control for the kit is recovering low and may be out of range for...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 23, 2017· Philips Electronics North America Corporation

Recalled Item: IntelliVue Multi Measurement Server Recalled by Philips Electronics North...

The Issue: Distorted ST-Segment when using 12-Lead ECG Monitoring with Philips...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2017· Siemens Medical Solutions USA, INC

Recalled Item: Artis oneFloor-mounted system for uncompromised imaging Recalled by Siemens...

The Issue: The possibility exists for the monitor display of Artis one systems with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2017· Zimmer Biomet, Inc.

Recalled Item: Ziptight Ankle Syndesmosis Fixation Device Recalled by Zimmer Biomet, Inc....

The Issue: Ziptight Ankle Syndesmosis Fixation was packaged without the tip protectors.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...

The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 22, 2017· Smiths Medical ASD Inc.

Recalled Item: Medfusion Recalled by Smiths Medical ASD Inc. Due to Potential for the...

The Issue: Potential for the syringe barrel clamp mechanism to loosen, decreasing the...

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

Class II — Potential Health HazardOngoing
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Q.Care Oral Cleansing & Suctioning System Suction Toothbrush Compatible with...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Toothette Oral Care Daily Oral Cleansing Kit Petite Size with Recalled by...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugAugust 22, 2017· Sage Products Inc

Recalled Item: Q Care RX Petite Oral Cleansing & Suctioning System with Recalled by Sage...

The Issue: Cross Contamination With Other Products: Oral care solutions were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund