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. 2,856 recalls have been distributed to California in the last 12 months.
Showing 23081–23100 of 30,923 recalls
Recalled Item: MEVION S250 Radiation therapy system Recalled by Mevion Medical Systems,...
The Issue: The treatment table positioning belt can slip gear positions, resulting in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dressol-X Recalled by Rainbow Specialty & Health Products Due to Rainbow...
The Issue: Rainbow Specialty & Health Products initiated a field action for Dressol-X...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software version VD10E for Syngo X-Workplace Recalled by Siemens Medical...
The Issue: Potential post-processing software issue when using tabcard "4D" on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Fuhrman Pleural/Pneumopericardial Drainage Set The Fuhrman...
The Issue: Stryker Sustainability Solutions is recalling the Fuhrman Pleural &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Integral Centralizer Hip System Recalled by Biomet, Inc. Due to PMMA...
The Issue: PMMA is listed as a material on the label but the product does not contain PMMA.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer K2 EDTA (K2E) 5.4mg Plus Blood Collection Tubes. Recalled by...
The Issue: Some tubes were manufactured with the stopper not fully inserted into the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MediChoice Cohesive Bandages Recalled by Owens & Minor Distribution, Inc....
The Issue: MediChoice sterile cohesive bandages imported and sold under a private brand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lumenis M22 System Model Number: GA-0005400 (M22 IPL + YAG Recalled by...
The Issue: Lumenis Ltd Announces a Field Action of the M22 IPL Acne Filters for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Recalled by Zimmer Biomet, Inc. Due to Zimmer Biomet is initiating a...
The Issue: Zimmer Biomet is initiating a recall of the Virage Occipital Eyelet, as it...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Imaging XS is a Picture Archiving and Communication System (PACS)...
The Issue: For the Syngo Workflow SLR System with Software Ver: VB10C: Printouts may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Olympus ENDOEYE HD II Video Telescopes. Models WA50040A ENDOEYE HD II...
The Issue: A damaged temperature sensor at the ENDOEYE tip caused the distal end to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugSmart Dip (MET/OPI2)+AMP+BZO+COC+THC Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProScreen 9 Panel Cup w/Adulterants Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Immutest 5 Pnl Drug Cup w/ Adult -waived Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProScreen 12 Drug Cup w/Adulteration Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ProScreen 8 Panel Dip Card w/Adult Recalled by Ameditech Inc Due to...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iCup DX 12 Panel w/ Adulterant Recalled by Ameditech Inc Due to Ameditechs...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DrugSmart 11 Test Cup Recalled by Ameditech Inc Due to Ameditechs Drugs of...
The Issue: Ameditechs Drugs of Abuse Tests listed above have shown reduced reactivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.