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. 2,839 recalls have been distributed to California in the last 12 months.
Showing 29221–29240 of 56,506 recalls
Recalled Item: Pain Out Thai Kratom all packages Recalled by Nutrizone LLC Due to Potential...
The Issue: Dietary supplements have the potential to be contaminated with Salmonella.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Manischewitz Brand Recalled by R.A.B. Food Group LLC Due to Undeclared Allergen
The Issue: The R.A.B. Food Group LLC dba The Manischewitz Company, 80 Avenue K, Newark,...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chocolate Sea Salt Probiotic Granola Recalled by purely elizabeth. Due to...
The Issue: Chocolate Sea Salt Probiotic Granola due to undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Chlorhexidine Gluconate Oral Rinse Recalled by Akorn, Inc. Due to Subpotent...
The Issue: Subpotent Drug: Product crystallization with accompanying low out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 24-HOUR Oral Care q4 Kit with Ballard* Technology Recalled by Akorn, Inc....
The Issue: Subpotent Drug: Product crystallization with accompanying low out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 24-HOUR Oral Care q2 Kit with Ballard* Technology Recalled by Akorn, Inc....
The Issue: Subpotent Drug: Product crystallization with accompanying low out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Zhong Hua Jiu (menthol 1%) Patch Recalled by United Pacific Co Ltd Due to...
The Issue: CGMP Deviations: the product was produced with substandard GMP manufacturing...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Coronary Sinus (CS) Uni-Directional Diagnostic Electrophysiology (EP)...
The Issue: Thrombogenicity test results demonstrated that both the test devices (SSS)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery IGS 740 Interventional Fluoroscopic X-ray Systems Recalled by GE...
The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Discovery IGS 730 Interventional Fluoroscopic X-ray Systems Recalled by GE...
The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Innova IGS 630/520/530/540 Interventional Fluoroscopic X-ray Systems...
The Issue: The Discovery IGS and Innova IGS systems may experience X-ray abort errors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental System Proximal Femoral Component 38mm Offset Recalled by...
The Issue: There is a potential for debris in the hole on the superior lateral aspect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Connecting Tube - Female to Male Luer Lock Recalled by Cook Inc. Due to...
The Issue: Cap-adapter assembly of the device may potentially not be adequately...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...
The Issue: Specific lots of the device were overexposed during EtO sterilization. This...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.