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. 2,851 recalls have been distributed to California in the last 12 months.
Showing 24681–24700 of 30,923 recalls
Recalled Item: RECLAIM Assembled Implant Inserter Adaptor orthopedic manual surgical...
The Issue: This lot of the RECLAIM Assembled Implant Inserter Adaptor Instrument may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Inc. Cardiac Rhythm Disease Management Due...
The Issue: Clinicians observed debris, appearing to originate from the hemostasis valve...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobius3D Product Usage: Mobius3D software is used for quality assurance...
The Issue: Mobius3D version 1.5.0 contained a defect in software code which affects...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiMedica Catalys Precision Laser System Recalled by Abbott Medical Optics,...
The Issue: Device may experience loss of suction during treatment resulting in scoring...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Coblator II System Recalled by ArthroCare Medical Corporation Due to The...
The Issue: The recalling firm was notified by the contract manufacturer that they had...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endo TCS Driver Straight Hexalobe #6 P/N 5210-1004 Recalled by TITAN SPINE,...
The Issue: The TCS Straight Hexlobular #6 Drivers (5210-1004) tip sheared off during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Catalys Precision Laser System-Catalys - U - US product Recalled by...
The Issue: Software anomaly on OptiMedica CATALYS System version 3.00.05 that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008Kathome - 190895 2008T GEN 2 Recalled...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008T with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008K with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 Series Hemodialysis Machines: 2008K2 with the following product code...
The Issue: The Acetate value for GranuFlo on the Select Concentrate screen should be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GAP Nail 4.8mm (diameter size) of the GAP ENDO-EXO MEDULLARY Recalled by...
The Issue: Failures of the 4.8mm of the GAP Endo-Exo Medullary System have been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermoFlo 1 HME Recalled by Arc Medical Inc Due to Outer shipping carton was...
The Issue: Outer shipping carton was marked with an incorrect expiry date, however...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMSCO C and AMSCO 400 Steam Sterilizers Recalled by Steris Corporation Due...
The Issue: STERIS has identified that the control board software in select AMSCO 400...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Caviwave Pro Ultrasonic Cleaning System Recalled by Steris Corporation Due...
The Issue: Should the Caviwave Pro Ultrasonic Cleaning System experience a temporary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Q-Syte Luer Access Split Septum Recalled by Becton Dickinson & Company...
The Issue: Becton Dickinson received an elevated number of complaints for blood or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Spirit TM Select bed is a Med-Surg bed intended Recalled by CHG Hospital...
The Issue: It was identified that in some situations the bed exit alarm may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Double Swivel Connector with Suction Port Connector Recalled by King Systems...
The Issue: Product is mislabeled as Double Swivel Connector with Suction Port and is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thumb Screw for the Synthes Recon Locking Aiming Arm for Recalled by...
The Issue: For certain lots, the incorrect raw material of annealed 17-4PH Stainless...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Transonic Hemodialysis Monitor Recalled by Transonic Systems Inc Due to...
The Issue: Customer unable to obtain measurements due to the device seeing no flow or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.