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. 2,669 recalls have been distributed to California in the last 12 months.
Showing 41981–42000 of 56,506 recalls
Recalled Item: Perkin Elmer WIZARD2 5-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Medley LVP Frame Membrane. Intended use to hold platen Recalled by...
The Issue: Administration of inappropriate quantities of fluid can result, with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perkin Elmer WIZARD2 1-detector Recalled by Perkinelmer Due to Error in...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Medley LVP Bezel Assembly. Intended use to hold platen Recalled by...
The Issue: Administration of inappropriate quantities of fluid can result, with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WIZARD2 2-detector Recalled by Perkinelmer Due to Error in WIZARD2 Barcode...
The Issue: Error in WIZARD2 Barcode ID Label #023 Content may produce erroneous results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Femoral Drill Guide Lateral IM Adapter Product Usage: Drill Recalled...
The Issue: Oxford Femoral Drill Guide Lateral IM Adapter may have an undersized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SERFAS 90 degree Energy Probe Recalled by Stryker Endoscopy Due to Stryker...
The Issue: Stryker Endoscopy is recalling all non expired SERFAS 90 degree Energy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heparin Sodium and 0.9% Sodium Chloride Injection Recalled by Baxter...
The Issue: Subpotent Drug; out of specification results for heparin raw material
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...
The Issue: Multiple dietary supplement regulation violations.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...
The Issue: Marketed without an approved NDA/ANDA - Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Smart Lipo Dietary Supplement capsules Recalled by Centro Naturista Due to...
The Issue: Marketed without an approved NDA/ANDA - Product contains undeclared...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Eating Right Black Bean Soup Recalled by San Francisco Spice Company, Inc....
The Issue: Some containers or Eating Right Black Bean Coup may contain Eating Right...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: EVac 70 XTRA with Integrated Cable and PROcise EZ View Recalled by...
The Issue: Wands inspected with the adaptor fixture were released to the field not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurus 2500 Standalone Vitreous Probe Recalled by Alcon Research, Ltd. Due...
The Issue: Insufficient seal on the outside packaging, potentially affecting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker SelectCore Variable Throw Biopsy Device Recalled by Stryker...
The Issue: Stryker Instruments is recalling the Stryker SelectCore Variable Throw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitatrim Injection Recalled by The Compounding Pharmacy of America Due to...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tri-Mix (37.5/2/20) (MFG) Injectable Recalled by The Compounding Pharmacy of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydromorphone 15 mg/ml Solution Recalled by The Compounding Pharmacy of...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Testosterone Cypionate 250 mg/ml Injection Recalled by The Compounding...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Tri-Mix ST4 (3 mg/1.5 mg/300 mcg) Injectable Recalled by The Compounding...
The Issue: Lack of Assurance of Sterility; FDA inspection identified GMP violations...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.