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. 1,043 recalls have been distributed to California in the last 12 months.
Showing 42421–42440 of 56,506 recalls
Recalled Item: Infinite M1000 PRO in vitro diagnostic. Product Usage: The Tecan Recalled by...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2100IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova IGS 520. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Innova 2121IQ. Angiographic X-ray systems used in generating...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima CL 323i. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Discovery IGS 730. Angiographic X-ray systems used in Recalled...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infinite F500 Recalled by Tecan US, Inc. Due to A firmware bug causes...
The Issue: A firmware bug causes incorrect values to be displayed for specific measured...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Optima IGS 320. Angiographic X-ray systems used in Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue that may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triathlon PS X3 Tibial Insert Recalled by Stryker Howmedica Osteonics Corp....
The Issue: Stryker Orthopaedics received a report that 5537-G-319 No 3. Triathlon TS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Enalapril maleate and hydrochlorothiazide tablets USP Recalled by Apotex...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Losartan potassium tablets USP Recalled by Apotex Inc. Due to Failed Content...
The Issue: Failed Content Uniformity Specifications: The product may not meet the limit...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reamer / Irrigator / Aspirator (RIA): RIA Drive Shafts Recalled by Synthes,...
The Issue: It was reported that the RIA Drive Shaft, Tube Assembly, and Reamer Head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tool Recalled by American Medical Systems Innovation Center - Silicon Valley...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sureflex 200 Lithotripsy Fiber Recalled by American Medical Systems...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fiber Stripper Recalled by American Medical Systems Innovation Center -...
The Issue: validation data related to cleaning instructions and sterilization methods...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.