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. 2,881 recalls have been distributed to California in the last 12 months.
Showing 20801–20820 of 30,923 recalls
Recalled Item: Arsenal Spinal Fixation System Recalled by Alphatec Spine, Inc. Due to...
The Issue: Alphatec Spine is recalling the Arsenal Spinal Fixation System Set Screw due...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZWAY 8F STRAIGHT S79CM D84CM Catalog # AB081211 Recalled...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEDTRONIC ARRIVE BRAIDED TRANSSEPTAL SHEATH 10F C120¿ S61CM D66CM GLOBAL...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products Intact PTH Reagent Pack: 1) UPN...
The Issue: The device defect is a positive bias of up to 20% relative to the currently...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR BREEZEWAY 10F S60.8CM D65.6CM FIRM TIP Catalog # AB1061FT Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZEWAY 10F C55¿ S79CM D84CM Catalog # AB101076 Recalled by...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSCOR ADELANTE BREEZWAY 10F STRAIGHT S79CM D84CM Catalog # AB101219 Recalled...
The Issue: Complaint that during insertion of the dilator through the sheath a fragment...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tina-Quant Hemoglobin A1c Gen. 2 Hemoglobin A1c test Catalog number Recalled...
The Issue: Roche Diagnostics has confirmed elevated QC and patient sample recovery for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: COBAS INTEGRA 800 Tina-Quant Hemoglobin A1cDX Gen.2 Hemoglobin A1cDX test...
The Issue: .Roche Diagnostics has confirmed elevated QC and patient sample recovery for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Clearify Visualization System Item Code: 21-345 Intended to be...
The Issue: Product sterility is compromised due to breach of the sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Best Practices kits containing certain production lots of Clearify...
The Issue: Product sterility is compromised due to breach of the sterile barrier
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Normal Saline Flush 0.9% USP Sodium Chloride Injection Syringe Recalled by...
The Issue: Potential contamination with B. cepacia.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic SynchroMed II Implantable Drug Infusion System. This system...
The Issue: Medtronic is following up to a May 2013 communication regarding the Priming...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0 mm Reaming Rod/950 mm w/straight Ball Tip Recalled by Synthes (USA)...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TBS iNsight Version v.3.0.1 Product Usage: TBS iNsight is a Recalled by...
The Issue: The FRAX adjusted for TBS values are not correct when: The FRAX feature is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Guide Rod w/Smooth Tip 950 mm Recalled by Synthes (USA) Products LLC...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm TI Calibrated Reaming Rod 850 mm Recalled by Synthes (USA) Products...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod W/Ball Tip 650 mm Recalled by Synthes (USA) Products LLC...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0 mm Guide Rod/950 mm with Smooth Tip Recalled by Synthes (USA) Products...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod with Ball Tip & Extension/950 mm Recalled by Synthes...
The Issue: The peel pouches for the affected reaming rods and extraction hooks are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.