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. 1,204 recalls have been distributed to California in the last 12 months.
Showing 8481–8500 of 56,506 recalls
Recalled Item: VITROS XT 3400 Chemistry System Product Code 6844458 Running Software...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to Pump not...
The Issue: Pump not detected as connected to controller due to software issue.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System Product Code 6802783 and Product...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Product Code 6844461 Running Software...
The Issue: During planned monitoring of data post-release of Software Version 3.8.0 an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stay Safe Cap Recalled by Fresenius Medical Care Holdings, Inc. Due to...
The Issue: Updating the labeling to include additional warnings and contraindications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Automated Impella Controller (AIC) Recalled by Abiomed, Inc. Due to Pump not...
The Issue: Pump not detected as connected to controller due to software issue.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MED-810A Zemits NDPrime Laser products Recalled by Advance-Esthetic LLC Due...
The Issue: Advance-Esthetic LLC failed to comply with the applicable standards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips EPIQ Diagnostic Ultrasound System Models: EPIQ 7G(model # 795200)...
The Issue: Their is the potential that diagnostic ultrasound systems operating with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Affiniti 70 Recalled by Philips Ultrasound, Inc. Due to Their is the...
The Issue: Their is the potential that diagnostic ultrasound systems operating with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology with software version V4.8.0.10421...
The Issue: For oncology users: If the user performed off-set reconstruction on CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT on Rails Recalled by Philips North America Due to When preparing...
The Issue: When preparing for CCT Fluoroscopy mode and activating the CCT foot pedal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Big Bore RT with software version V4.8.0.10421- Model: 728242 CT Recalled by...
The Issue: For oncology users: If the user performed off-set reconstruction on CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT Big Bore with software version V4.8.0.10421 Model:728244 CT...
The Issue: For oncology users: If the user performed off-set reconstruction on CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Segmental Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spectral CT on Rails Recalled by Philips North America Due to This recall is...
The Issue: This recall is part of a 2-issue recall for the same system. When using the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Compress Device Short Anchor Plug Recalled by Biomet, Inc. Due to Anchor...
The Issue: Anchor plugs potentially have metal burrs in the transverse holes of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.