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. 2,867 recalls have been distributed to California in the last 12 months.
Showing 21861–21880 of 30,923 recalls
Recalled Item: HeartStart MRx Monitor/Defibrillator The HeartStart MRx is for use for...
The Issue: MRx monitor/defibrillators could fail to charge because the therapy printed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Dynamics Recalled by Siemens Medical Solutions USA, Inc Due to Siemens...
The Issue: Siemens has identified changes in default carry forward workflow using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CytoScan¿ Dx Assay. The CytoScan Dx Assay consists of five reagent modules...
The Issue: During a recent Ohio site inspection by the FDA it was discovered that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Vented Dispensing Pin with Luer Lock Ultrasite Valve Product Usage:...
The Issue: BBMI recently identified a potential for a tear in the outer blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MEXL-3010/A5- Vantage Titan 3T Magnetic Resonance Imaging System Product...
The Issue: A potential problem associated to the gradient coil (ASGC) in the Titan 3T...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magnesium on RX Imola analyser IVD Recalled by Randox Laboratories, Limited...
The Issue: According to the firm, Carry over was observed when the amylase or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite...
The Issue: BBMI recently identified a potential for a tear in the outer blister...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactate Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Uric Acid Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lipase Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cholesterol Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Triglyceride Recalled by Beckman Coulter Inc. Due to Beckman Coulter has...
The Issue: Beckman Coulter has identified that Dipyrone (Metamizole) may cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAGNETOM Aera/Skyra Systems Recalled by Siemens Medical Solutions USA, Inc...
The Issue: The docking station top cover of the removable patient table may contain a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Battery Pack Used with the Capnostream"20 and Capnostream"20p Patient...
The Issue: Medtronic Respiratory & Monitoring Solutions Announces a Voluntary Recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CinchLock Flex Knotless Anchor with Inserter Recalled by Stryker Corporation...
The Issue: Stryker Endoscopy is recalling the CinchLock SS Knotless Anchor with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CinchLock SS Knotless Anchor with Inserter Recalled by Stryker Corporation...
The Issue: Stryker Endoscopy is recalling the CinchLock SS Knotless Anchor with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUE 3D VIEWER SYSTEM Model Number EP-00001-XX Software versions 1.0...
The Issue: Imaging system data may be displayed with an incorrect orientation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVARREST Fibrin Sealant Patch Recalled by Ethicon, Inc. Due to Ethicon is...
The Issue: Ethicon is recalling EVARREST Fibrin Sealant Patch because the characters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PerFuse Decompression Instrument PN: 800-0541 Recalled by Biomet, Inc. Due...
The Issue: The Trocar and Plunger Assemblies are missing from the instrument, which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natus neoBLUE Phototherapy system Recalled by Natus Medical Incorporated Due...
The Issue: The firm is adding the warning statement to the Instruction for Use for the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.