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. 3,026 recalls have been distributed to California in the last 12 months.
Showing 7961–7980 of 56,506 recalls
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom procedural convenience kits and trays Recalled by American Contract...
The Issue: During an internal investigation, ACS identified that several components...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis Vibe Hemo Recalled by Siemens Medical Solutions USA, Inc Due to The...
The Issue: The possibility of the Sensis documentation functionality application to crash.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ivenix Infusion System (IIS) Recalled by Fresenius Kabi USA, LLC Due to The...
The Issue: The device may experience mechanical interference on the Fluid Valve pins,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MICRO-X Rover Mobile X-ray System Recalled by Micro-X Ltd. Due to Mobile...
The Issue: Mobile x-ray system can report and deliver a lower post-exposure mAs value...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Packaged Recalled by AtriCure, Inc. Due to AtriCure has identified certain...
The Issue: AtriCure has identified certain lots of tank hose assemblies where a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cryo Module Accessories Domestic CMA-OUS Recalled by AtriCure, Inc. Due to...
The Issue: AtriCure has identified certain lots of tank hose assemblies where a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Volar Bearing Plate. Recalled by TriMed Inc. Due to Plates, part of a wrist...
The Issue: Plates, part of a wrist fixation system, are affixed during surgery with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) Patient Information Center iX Recalled by Philips North America Due to...
The Issue: Push notifications may fail to send to the user under certain conditions....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) CareEvent Recalled by Philips North America Due to Push notifications...
The Issue: Push notifications may fail to send to the user under certain conditions....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VADER pedicle system Recalled by Icotec Ag Due to icotec has received...
The Issue: icotec has received notification of one revision that had to be carried out...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Navigation, Inc. Due to Their is the...
The Issue: Their is the potential that the percutaneous pin may have a cross-pin that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MYNXGRIP 5F Recalled by Cordis US Corp Due to Cordis became aware that the...
The Issue: Cordis became aware that the label for the carton box containing 10 units is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Navigation, Inc. Due to Their is the...
The Issue: Their is the potential that the percutaneous pin may have a cross-pin that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.