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. 3,072 recalls have been distributed to California in the last 12 months.
Showing 361–380 of 30,923 recalls
Recalled Item: The LDL-Cholesterol assay is comprised of two distinct phases. In Recalled...
The Issue: Beckman Coulter identified that LDL Cholesterol OSR6x96 is not meeting the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Azurion Systems R3.0. Includes the following label descriptions and...
The Issue: Nine (9) identified software issues which may result in the following: loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: HFD100 Product Name: Head Fixation Device HFD100 Model/Catalog...
The Issue: Torque screw may crack or separate. If used, an affected screw could lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial 900 MHz Call Station Recalled by Securitas Healthcare LLC Due to...
The Issue: Securitas Healthcare has become aware of a firmware issue in the Call...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arial 900 MHz Call Station Recalled by Securitas Healthcare LLC Due to...
The Issue: Securitas Healthcare has become aware of a firmware issue in the Call...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog...
The Issue: Incorrect expiration date
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Revogene C. difficile Recalled by Meridian Bioscience Inc Due to The...
The Issue: The affected lots show a decline in performance over time, which may lead to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Leos Laser and Endoscopy System. Model Number: OME6000U. Recalled by...
The Issue: Manufacturing deviation in which the ferrites specified for the USB cable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allwell Inflation Device Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Inflation Device.basixCOMPAK.30 atm/bar.20 mL Numbers:...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merit Medical Recalled by Merit Medical Systems, Inc. Due to Inflation...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allwell Angioplasty Pack /B Recalled by Merit Medical Systems, Inc. Due to...
The Issue: Inflation device handle may detach from the syringe during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Ion Endoluminal System Product Name: Ion Vision Probe Recalled...
The Issue: Due to probe bags that may have a compromised or incomplete sterile pouch seal.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Detachable 10in Pend FRU-1 Pend component for the AIRO Computed Recalled by...
The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Detachable 10in Pendant Upgrade component for the AIRO Computed Tomography...
The Issue: AIRO pendant replacement kits and upgrade do not possess the "Safe Hand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Abre Venous Self-Expanding Stent System Recalled by Medtronic Inc Due to...
The Issue: Stents may be impacted by a Nitinol anomaly which causes a reduced stent...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ingenia Ambition S. Product Code (REF): 782108. MR systems with Recalled by...
The Issue: The potential for stiffness value errors when viewing exported MR...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.