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. 3,047 recalls have been distributed to California in the last 12 months.
Showing 4921–4940 of 30,923 recalls
Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...
The Issue: Their is the potential that Universal Clip applier may not load clip after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 NI/TU Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU Recalled by Angiodynamics, Inc....
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 5F X 10 CM STD .018 SS/SS Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Epix Universal Clip Applier Recalled by Applied Medical Resources Corp Due...
The Issue: Their is the potential that Universal Clip applier may not load clip after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MINI STICK MAX 4F X 10 CM STD .018 SS/PD Recalled by Angiodynamics, Inc. Due...
The Issue: Non-conformance may prevent the guidewire from passing through the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRI system: Vantage Elan Recalled by Canon Medical System, USA, INC. Due to...
The Issue: For some MRI systems, it has been found that some of the maximum Spatial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Embrace Drill Tower Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due...
The Issue: The surgical techniques for the Embrace Shoulder Instruments -Drill Tower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MRI system: Vantage Orian Recalled by Canon Medical System, USA, INC. Due to...
The Issue: For some MRI systems, it has been found that some of the maximum Spatial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NxStage Cartridge Express with Speedswap Recalled by NxStage MDS Corporation...
The Issue: Product is recalled due to reports of blood leaking or spraying from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Embrace Drill Tower Recalled by Waldemar Link GmbH & Co. KG (Mfg Site) Due...
The Issue: The surgical techniques for the Embrace Shoulder Instruments -Drill Tower...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vantage Titan Recalled by Canon Medical System, USA, INC. Due to For some...
The Issue: For some MRI systems, it has been found that some of the maximum Spatial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Shimadzu Recalled by SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Due to...
The Issue: Due to capacitor manufacturing issue, their is a potential that Flat Panel...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IdentiTi ALIF Standalone Interbody System: Part Number/Description...
The Issue: Due to reports of intraoperative graft bolt implantation breakages.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT 7600 Integrated System Recalled by Ortho-Clinical Diagnostics,...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System Catalog Nos. 6802445 (regular) and 6900440...
The Issue: A software defect affecting VITROS Systems running VITROS Software Versions...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.