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 23961–23980 of 30,923 recalls
Recalled Item: CentraLink" Data Management System Recalled by Siemens Healthcare...
The Issue: Siemens Healthcare Diagnostics has determined that the sample query function...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaTREK Instrument Series 240 Recalled by Remel Inc Due to Use of the...
The Issue: Use of the recalled product may result in false positive reports.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur Tni-Ultra Assay Recalled by Siemens Healthcare Diagnostics,...
The Issue: System-to-system bias between the Tni-Ultra assay on the ADVIA Centaur CP...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pointe Scientific G6PD Controls Kit configuration: 6 x 0.5 ml Recalled by...
The Issue: A reduction in the reconstituted stability has been identified. Clinicians...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaTREK Instrument Series 528 Recalled by Remel Inc Due to Use of the...
The Issue: Use of the recalled product may result in false positive reports.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOFIX Firebird Spinal Fixation System 6.5mm x 55mm Multi-Axial Screw...
The Issue: The Firebird Spinal Fixation System 6.5 mm x 55 mm Bone Screw, Self-Tapping...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ally Uterine Positioning System (Ally UPS) used in the mounting Recalled by...
The Issue: Design of device may expose user to injury to fingers or body parts
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ClearSight Recalled by Edwards Lifesciences, LLC Due to Edward Lifesciences...
The Issue: Edward Lifesciences is recalling the ClearSight System because the finger...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: M/L Taper with Kinectiv¿ Technology. prosthesis Recalled by Zimmer, Inc. Due...
The Issue: Zimmer is initiating a voluntary recall of 64 lots (752 implants total) of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVAC 70 XTRA with Integrated Cable Product Usage: Recalled by ArthroCare...
The Issue: Potential component failure causing device inoperability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PROcise XP Wand with Integrated Cable Product Usage: Recalled by ArthroCare...
The Issue: Potential component failure resulting in inoperability
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cell Search Circulating Tumor Kit. Intended for the enumeration of Recalled...
The Issue: Complaints of the presence of artifacts that appears as small bead like...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Ultrasound Recalled by Philips Ultrasound, Inc. Due to Philips...
The Issue: Philips Healthcare has discovered a problem in the Philips Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedTest DX Control Reconstitution Fluid Kit configuration: 20 x 5 Recalled...
The Issue: Vial to vial variation in the fill volume that could affect control recovery...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via and Syngo.x Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: measurements drawn on the 2nd and subsequent images of the series are not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lifesaver Single Patient Use Manual Resuscitator Product Usage: The Hudson...
The Issue: The intake port may be blocked which can cause the bag to fail to fill.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LapSac Surgical Tissue Pouch. The current intended use for the Recalled by...
The Issue: Includes Information not stated in the intended use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Optigun Ratchet is a hand-held cement gun for use Recalled by BIOMET...
The Issue: The pin which maintains the knob button, may disconnect and become lost....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The spare component Anti-HBs Cutoff Calibrator Recalled by Bio-Rad...
The Issue: The spare component Anti-HBs Cutoff Calibrator, Catalog number 26154, is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Extentrac Elite User Manual DCN: 14-001 (Powered decompression table...
The Issue: Item is marketed for use in patients weighing up to 350 lbs, but the device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.