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 23141–23160 of 30,923 recalls
Recalled Item: DrugSmart Dip AMP/OPI2/COC/THC/BZO Test 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 8 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: ProScreen 6 Panel Dip Card w/Adult (AU) 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 Panel Dip Card 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: ProScreen 10 Panel 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.
Recalled Item: ProScreen 10 Panel Dip Card 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: ProScProScreen 10 Panel Cup with Adulterants Recalled by Ameditech Inc Due...
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: BIRMINGHAM HIP RESURFACING MODULAR HEAD Recalled by Smith & Nephew, Inc. Due...
The Issue: The 16 devices distributed in the United States were incorrectly labeled as...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iCup DX 11 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: 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: DrugSmart 9 Test Cup (BUP) Recalled by Ameditech Inc Due to Ameditechs Drugs...
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 6 Panel Cassette w/Adult (AU) 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: Radiographic Transparency for Certain and External Connection Tapered...
The Issue: Images contained within radiographic transparency ART 1036 are undersized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EDI BZO Uncut Sheet - Cup* Recalled by Ameditech Inc Due to Ameditechs Drugs...
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: 6 Panel Cup Body and Lid w/Adult (AU) 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: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...
The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Chloride Inhalation Solution Recalled by Nephron Pharmaceuticals...
The Issue: Lack of Assurance of Sterility: Internal dye ingress test failure to assure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Recalled by STERILMED, INC. Due to Sterilmed, Inc. is voluntarily...
The Issue: Sterilmed, Inc. is voluntarily recalling all unexpired Reprocessed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima IGS 320. Product Usage: The angiographic X-ray Recalled...
The Issue: GE Healthcare has recently become aware of a potential safety issue related...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maquet HCU 30 Coolant Type R134A Filling weight 250 g Recalled by Maquet...
The Issue: Failure of the HEATER-COOLER UNIT (HCU 30) Type 2 power supply board. A drop...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.