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. 1,243 recalls have been distributed to California in the last 12 months.
Showing 1881–1900 of 56,506 recalls
Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ Hydrogel Adhesive Sheet...
The Issue: Packaging failures were identified which could lead to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: t:slim X2 insulin pump with Interoperable Technology Recalled by Tandem...
The Issue: A software defect in versions 7.9.0.1 and 7.10.1 of the pump software for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensodyne PRONAMEL (Potassium nitrate 5% Recalled by Haleon US Holdings LLC...
The Issue: Labeling: Label Mix-up: The outer carton is labelled Fresh Mint. The tube is...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: MediHoney¿ Product Name: MediHoney¿ Hydrogel Model/Catalog...
The Issue: Packaging failures were identified which could lead to a breach in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Alcon Laboratories Recalled by Alcon Research LLC Due to Due to...
The Issue: Due to incomplete seals in the pouch which provide the sterile barrier.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for open header bag...
The Issue: Potential for open header bag seals, compromising sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Halyard Recalled by AVID Medical, Inc. Due to Potential for open header bag...
The Issue: Potential for open header bag seals, compromising sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactated Ringer's Injection USP Recalled by B BRAUN MEDICAL INC Due to Lack...
The Issue: Lack of Assurance of Sterility; potential for fluid leakage at one of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B BRAUN MEDICAL INC Due to...
The Issue: Lack of Assurance of Sterility; potential for fluid leakage at one of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vial Label: Epinephrine Injection Recalled by PFIZER INC Due to Lack of...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vial Label: 8.4% Sodium Bicarbonate Injection Recalled by PFIZER INC Due to...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: PhD Hemostasis Valve Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Hemostasis valve has a manufacturing defect and when used the valve cap may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sri Sri Tattva Recalled by SRI SRI TATTVA Due to Undeclared Soy
The Issue: Product contains undeclared soy lecithin.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Interventional Fluoroscopic X-Ray System - Philips Allura Xper Series....
The Issue: Potential that a component (air baffle) may be missing in some Nehalem...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion System configured with a 1 Phase UPS. Azurion family (R1.x...
The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Allura System configured with a 1 Phase UPS. Allura family (R1.x...
The Issue: Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.