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. 1,217 recalls have been distributed to California in the last 12 months.
Showing 3461–3480 of 30,923 recalls
Recalled Item: IMMAGE Immunochemistry Systems IGM Immunoglobulin M Reagent IGM Recalled by...
The Issue: Firm identified two lots of reagents that are not meeting the sensitivity...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stainless Steel Sims Uterine Sound Recalled by CooperSurgical, Inc. Due to...
The Issue: During the manufacturing process the devices were laser-marked with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspire Model 4340 Respiratory Sensing Lead Recalled by Inspire Medical...
The Issue: Labeling error with a mismatch between the shelf box serial number label and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed 630G Insulin Pump Recalled by Medtronic MiniMed, Inc. Due to Insulin...
The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MiniMed Insulin Pump Device. MiniMed 670G Recalled by Medtronic MiniMed,...
The Issue: Insulin pumps that have been dropped, bumped, or experienced physical impact...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Silver-Plated Copper Sims Uterine Sound Recalled by CooperSurgical, Inc. Due...
The Issue: During the manufacturing process the devices were laser-marked with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ Total Bilirubin (TBIL) Flex Reagent Cartridge Recalled by...
The Issue: During manufacturing, the last three tests from the 160 test flex of lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DR 800. Digital Radiography X-ray System. Recalled by Agfa N.V. Due to...
The Issue: Potential for the front lever chain of the DR 800 table to fail.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by Siemens...
The Issue: The potential for biased quality control (QC) and patient results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein (UCFP) Recalled by...
The Issue: The potential for biased quality control (QC) and patient results when using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BiomarC EX Fiducial Marker System Recalled by Carbon Medical Technologies,...
The Issue: This recall has been initiated due to a failure to provide an MRI Insert...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Recalled...
The Issue: Due to a voluntary recall of low dead space syringes, and luer slip tip...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.