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. 2,851 recalls have been distributed to California in the last 12 months.
Showing 24501–24520 of 30,923 recalls
Recalled Item: Artis Q/ Q zen systems Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: potential issue with the Artis Q/ Q zen systems where it is possible that an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LOW PROFILE NON-LOCK SCREW Recalled by Biomet, Inc. Due to A Biomet...
The Issue: A Biomet investigation found that the Low Profile Non-Locking Screw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Head Holder shipped with Ingenuity Core Computed Tomography X-ray Systems....
The Issue: A head holder released for use with other CT systems but not yet qualified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Monopty Disposable Core Biopsy Instruments and Kits Recalled by Bard...
The Issue: Bard Peripheral Vascular is recalling the Bard Monopty Disposable Core...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Dual Chamber Temporary External Pacemaker Recalled by Medtronic...
The Issue: Possible performance issue when used with specific AA-sized (LR6) batteries....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD99 Catalog number PM008 AA Recalled by Biocare Medical, LLC Due to A drop...
The Issue: A drop in staining intensity over time has been observed. These lots may not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Head Holder shipped with Ingenuity CT Computed Tomography X-ray Systems...
The Issue: A head holder released for use with other CT systems but not yet qualified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: American Catheter / Cholangiogram Catheter 9100 Series. Recalled by American...
The Issue: Catheters were not sealed before sterilization. and was not detected through...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Head Holder shipped with Ingenuity Core 128 Computed Tomography X-ray...
The Issue: A head holder released for use with other CT systems but not yet qualified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DiaSorin Recalled by Diasorin Inc. Due to Instability in the PRO-Trac II...
The Issue: Instability in the PRO-Trac II Tacrolimus ELISA kit which may cause falsely...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ebola Accessories assembled Recalled by Lusys Laboratories, Inc. Due to...
The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Denali Filter-Jugular/Subclavian DL950J Denali Filter-Femoral Delivery...
The Issue: IFU missing contraindications: Patients with uncontrolled sepsis and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Introduction Pack. A device inserted into an endotracheal tube to Recalled...
The Issue: Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ebola Virus GP-VP IgS Recalled by Lusys Laboratories, Inc. Due to LuSys...
The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ebola Virus Antigen Nasal Recalled by Lusys Laboratories, Inc. Due to LuSys...
The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nuclear Gamma Cameras (ADAC Vertex Classic Recalled by Philips Medical...
The Issue: During clinical use of a Vertex Plus Gamma Camera, as the detector heads...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pluer-evac Sahara Chest Drainage System Recalled by Teleflex Medical Due to...
The Issue: Package contains incorrect sized unit: The adult sized S-1100-08LF product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ebola IgX VP-40 Serum/Plasma/Blood Cassette Recalled by Lusys Laboratories,...
The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ebola GP IgM Blood (Blood Serum/Plasma/Cassette) Recalled by Lusys...
The Issue: LuSys Laboratories is recalling Ebola Virus One Step Test Kits to stop and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CareFusion Vital Signs LightWand Stylet. A device inserted into an Recalled...
The Issue: Vital Signs Colorado (dba CareFusion) is recalling Vital Signs LightWand...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.