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. 1,781 recalls have been distributed to California in the last 12 months.
Showing 7201–7220 of 30,923 recalls
Recalled Item: Plato 17 Microcatheter: Straight Tip Recalled by Scientia Vascular, Inc. Due...
The Issue: Microcatheters for embolic coil and diagnostic agent introduction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Micro-Fine IV Needle 1 ml Recalled by Becton...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Ultra-Fine Insulin Syringe 1mL Recalled by Becton Dickinson & Company Due...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In Vitro Diagnostic (IVD) Panel BioFire BCID2 Panel - Recalled by BioFire...
The Issue: Due to temperature excursions with products (products being stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In Vitro Diagnostic (IVD) Panel BioFire Respiratory Panel 2.1 (RP2.1)...
The Issue: Due to temperature excursions with products (products being stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Insulin Syringes with the BD Micro-Fine TM IV Needle 1ml Recalled by...
The Issue: Nonsterile syringe potentially exposing the patient to pathogenic...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: In Vitro Diagnostic (IVD) Panel FilmArray GI Panel - Recalled by BioFire...
The Issue: Due to temperature excursions with products (products being stored outside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PREAT NOBIL GRIP Recalled by Preat Corp Due to Product is labeled with an...
The Issue: Product is labeled with an incorrect expiration date.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Heartsine Samaritan PAD: SAM 350P semi-automatic defibrillator Recalled by...
The Issue: Automated external defibrillators were potentially distributed with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIOPHEN Protein C 5 kit is for in vitro quantitative Recalled by Aniara...
The Issue: New warnings and precautionary statements on product labelling: Reagent 2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Baxter MiniCap Disconnect Cap with Povidone-Iodine Solution Recalled by...
The Issue: MiniCap Disconnect Cap with Povidone-Iodine are packaged in foil pouches,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fusion Bioline Vascular Graft Recalled by Maquet Cardiovascular, LLC Due to...
The Issue: One (1) Fusion Bioline Vascular graft from lot 25162546, which failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD5 Series of Genesis Reusable Rigid Sterilization Container Systems catalog...
The Issue: Product did not meet shelf-life testing requirements resulting in a breach...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa COVID-19 Direct Recalled by DiaSorin Molecular LLC Due to Direct...
The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa Flu A/B & RSV Direct Gen II Recalled by DiaSorin Molecular LLC Due...
The Issue: Direct amplification Discs , used with COVID-19 and Flu A/B & RSV assays,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX-Compass/DR-FIT X-ray Systems with Firmware version 2.3.2.0/2.3.2.4. For...
The Issue: After pressing and releasing the Z-Axis Motorized buttons on the Tube Head...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Tacrolimus (TAC) Flex reagent cartridge-In vitro diagnostic test...
The Issue: Siemens Healthineers has received customer complaints and confirmed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Total Protein II- In vitro diagnostic use in Recalled by Siemens...
The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH LDL Cholesterol Direct (DLDL)-In vitro diagnostic quantitative...
The Issue: Reagent Carryover from LDL Cholesterol Direct (DLDL), Total Protein II (TP),...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.