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 23481–23500 of 30,923 recalls
Recalled Item: Access Free T3 Reagent Kit Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter, Inc. is recalling Access Free T3 Reagent Kit because they...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System: iUNI G2 Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConFormis iTotal CR Knee Replacement System- iTOTAL CR Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iUni Unicondylar Knee Replacement System- iUNI G2 Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iUNI Unicondylar Knee Replacement System iUNI G2 Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: XiO Radiation Treatment Planning System. Used to create treatment plans...
The Issue: Incorrect Treatment Delivery Using Third Party Fixed Wedges.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConFormis iDUO G2 Recalled by ConforMIS, Inc. Due to May contain small...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS Unicondylar Knee Replacement System iUNI G2 Recalled by ConforMIS,...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iDuo Bicompartmental Knee Replacement System iDUO G2 Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iDuo Knee Bicompartmental Knee Replacement System Recalled by...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConFormis iTotal Posterior Stabilized Knee Replacement System- ITOTAL...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ConForMIS iTotal CR (Cruciate Retaining) Knee Replacement System-iTOTAL CR...
The Issue: May contain small amounts of ethylene glycol residue
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Kits with Medtronic Covidien 0.9% Sodium Chloride Flush Syringes...
The Issue: Manufacturer of 0.9% Sodium Chloride Flush Syringes recalled due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Guide Wires for orthopedic procedures. Recalled by Zimmer, Inc. Due...
The Issue: Product labeling of these sterile guide wires (external carton label and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRIdian¿ ViewRay¿ Radiation Therapy System Recalled by Viewray Incorporated...
The Issue: ViewRay discovered that in the event that an encoder breaks or fails on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD4 (SK3) Recalled by Becton, Dickinson and Company, BD Biosciences Due to...
The Issue: CD4 FITC label contains an error in the Spanish small text - it states CD8 FITC.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Cholestech LDX Multianalyte Controls Recalled by Alere San Diego, Inc....
The Issue: Alere San Diego is recalling the Alere Cholestech LDX Multianalyte Control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD AffirM VPIII Microbial Identification Test Recalled by Becton Dickinson &...
The Issue: BD has confirmed that a portion of tests associated with the affected lots(...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThruPort Knot Pusher. This device is sold individually (Model KP1) Recalled...
The Issue: The configuration of the slot at the tip of the knot pusher may inhibit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Lab Data Manager System - Product Usage: syngo Lab Recalled by Siemens...
The Issue: Software Issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.