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 2041–2060 of 56,506 recalls
Recalled Item: STA-Liquid Anti-Xa 4. Model/Catalog Number: 00311US. The STA - Liquid...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA Satellite. Product Code: All . All software versions. The Recalled by...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STA-Liquid Anti-Xa 8. Model/Catalog Number: 00322US. The STA - Liquid...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: CELSITE Product Name: CELSITE BABYPORT SET PUR 4 Recalled by...
The Issue: The potential for minor injury such as damage to the vessel and/or tearing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parashore Pear Slices in Juice Recalled by W.W. Industrial Group, Inc. Due...
The Issue: Contaminated with elevated lead and cadmium
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Ascend Laboratories,...
The Issue: Failed Dissolution Specifications: low dissolution results
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Belsomra (suvorexant) tablets Recalled by Merck & Co. Inc Due to Failed...
The Issue: Failed Dissolution Specifications: potential for delayed dissolution of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: STA - Fibrinogen 5. Model/Catalog Number: 00674. The STA - Recalled by...
The Issue: Potential for contamination of STA-LIQUID ANTI-Xa by Stago Fibrinogen...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Ultra IABP Catheter Kit Product Name: Ultra IABP Recalled by...
The Issue: Device contains indications for use and device compatibility claims that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: DJO SURGICAL Product Name: ALTIVATE REVERSE WEDGE GLENOID...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: DJO SURGICAL Product Name: FA S Altivate Reverse Recalled by...
The Issue: Their is a potential that the reamer may kick or bind up during or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orthopedic Pack Recalled by O&M HALYARD INC Due to Surgical drape packs may...
The Issue: Surgical drape packs may have open seals, which may compromise the sterility...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SureStep Foley Tray System BARD¿ Lubri-Sil Foley Catheter Tray Recalled by...
The Issue: Foley catheter trays have incorrect inserts, user may think:1)Silicone, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PeriGiene Recalled by DermaRite Industries, LLC Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IPC Powerease System UDI-DI: 00613994448705 00643169406834. The IPC Recalled...
The Issue: Due to out of the box wobble of the driver.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KleenFoam Recalled by DermaRite Industries, LLC Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DermaSarra Recalled by DermaRite Industries, LLC Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DermaKleen Recalled by DermaRite Industries, LLC Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Drug Product: The products were found...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.