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.
Showing 28301–28320 of 30,923 recalls
Recalled Item: Getinge Assure Accufast BI Test Pack w/ 5 Controls Recalled by Steritec...
The Issue: Mesa Labs, based out of Bozeman, MT, informed SteriTec Products, Inc. of a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: nanoFLEX CC4204A Intraocular Lens Correct aphakia in persons 60 years...
The Issue: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Afinity CQ2015A Intraocular Lens The visual correction of aphakia in...
The Issue: STAAR Surgical Company is recalling a limited number of nanoFLEX CC4204A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System CR Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System PS Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System CPS Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Persona (TM) The Personalized Knee System UC Tibial Articular Surface...
The Issue: Zimmer had received complaints that reported breakage of the Persona Knee...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Si Vision System Cart Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Instrument Control Box Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Si Surgeon Side Cart Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: da Vinci Dual Camera Controller Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Factory testing on da Vinci Si Surgical Systems may not be in compliance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597106126 Provisional MIC POROUS PAT PROV 26MMX10MM Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597603110 Articular Surface AC ART SURF 34/STRIPED YEL 10 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Coiled Tube Infusors (Portable Elastomeric Infusion Systems)....
The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597601201 Femur CRA PRECOAT FEM COMP SIZE B/L Rx Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597602010 Articular Surface AC ART SURF 12/PUR 10 Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597502010 Provisional AC ART SURF PROV 12/PUR 10 Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Basal/Bolus Infusor. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.