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. 988 recalls have been distributed to California in the last 12 months.
Showing 50061–50080 of 56,506 recalls
Recalled Item: Fresenius Liberty¿ Cycler Part Number: RTLR180111 Product Usage: The Liberty...
The Issue: Fluid leaking may be observed inside the pump compartment of the Liberty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes 14.5 mm Outer Protection Sleeve for Suprapatellar Synthes 14.5...
The Issue: Complaints were received reporting that a product packaged as a 14.5 mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Multi Diagnost Eleva II Recalled by Philips Medical Systems, Inc....
The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Multi Diagnost Eleva with FlatDetector Recalled by Philips Medical...
The Issue: The possibility of the Air Kerma Rate for low dose mode will not be reduced...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Terrain Zyme LGS-Zyme (Z-12) Recalled by Innovative Labs, LLC Due to...
The Issue: Innovative Labs, LLC. has recalled two Dietary Supplements due to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Terrain Zyme Myco-Zyme (Z-13) Recalled by Innovative Labs, LLC Due to...
The Issue: Innovative Labs, LLC. has recalled two Dietary Supplements due to the...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Sterile Disposable Kit ( Contains Skin Tensioner ASY-25067 Recalled by...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epsilon Skin Tensioner:Rx Recalled by Restoration Robotics Due to Reports of...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTAS Disposable Kit ( Contains Skin Tensioner FP-45384 Recalled by...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTAS Disposable and Reuseable Kit ( Contains Skin Tensioner FP-45384...
The Issue: Reports of discoloration (residue) on the pins of the skin tensioner have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTERLOCKING IM SCREW 4.5 and INTERLOCKING IM SCREW LG Some Recalled by...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RECON SCREW LG 5.5MM DIA and M/DN FEM IM NAIL Recalled by Zimmer, Inc. Due...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System: One 1 g...
The Issue: Incorrect instructions for use (IFU).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUFILL¿ n-Butyl Cyanoacrylate (n-BCA) Liquid Embolic System Recalled by...
The Issue: Incorrect instructions for use (IFU).
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD GeneOhm Cdiff Assay Recalled by Becton Dickinson & Co. Due to An...
The Issue: An incorrect reagent was packed with an in vitro diagnostic kit, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERSA-FX KEYLESS 90D X 8 and X 11 Recalled by Zimmer, Inc. Due to Zimmer...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.5 COMP PLT Recalled by Zimmer, Inc. Due to Zimmer recently conducted a...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Vivid E9 ultrasound system. GE Vivid E9 is a Recalled by GE Healthcare,...
The Issue: GE became aware of a potential safety issue due to a system slow down and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISTAL MEDIAL FEMORAL CON Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZIMTRON 6 DEG 22 HEADS Recalled by Zimmer, Inc. Due to Zimmer recently...
The Issue: Zimmer recently conducted a review of all historic packaging validations at...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.