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. 3,022 recalls have been distributed to California in the last 12 months.
Showing 9361–9380 of 30,923 recalls
Recalled Item: SMART FLEX 6x150 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 10x100 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 10x100 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 8x60 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 9x60 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SMART FLEX 6x120 BIL Recalled by Cordis Corporation Due to There is a...
The Issue: There is a potential for distal tip dislodgement or separation.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .15.020 Recalled by Limacorporate S.p.A Due to There is a potential that the...
The Issue: There is a potential that the length of bone screws identified on labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: .15.010 Recalled by Limacorporate S.p.A Due to There is a potential that the...
The Issue: There is a potential that the length of bone screws identified on labeling...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MENTOR Saline-Filled Breast Implants are constructed from room temperature...
The Issue: Due to a manufacturing issue, Implant may have a potentially weakened area...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT i1000SR /1L86 and 1L87 Recalled by Abbott Laboratories Due to...
The Issue: Twelve software-related issues affecting software version 9.41 and earlier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT c4000 /2P24 Recalled by Abbott Laboratories Due to Twelve...
The Issue: Twelve software-related issues affecting software version 9.41 and earlier...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number: 909075...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number:...
The Issue: XXX
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Generator 220V Cooper Surgical Part Number: LP-20-220...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Integrated System Recalled by CooperSurgical, Inc. Due to...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Quantum 2000 Electrosurgical Generators Cooper Surgical Part Number:...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP PRECISION Generator 120V Cooper Surgical Part Number: LP-20-120...
The Issue: Coagulate function may not operate with the use of the Hand Switch, failure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemodialysis Delivery System Recalled by Baxter Healthcare Corporation Due...
The Issue: If the operator initiates therapy with a saved prescription profile and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc...
The Issue: Ancillary reagent packs used on Atellica IM 1300 and Atellica IM 1600...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.