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. 2,839 recalls have been distributed to California in the last 12 months.
Showing 29981–30000 of 30,923 recalls
Recalled Item: Philips and Laerdal brands of HeartStart HS1 Defibrillator Family Model...
The Issue: Philips determined that it is important to clarify information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 1 base 100/120V The Terumo Advanced Perfusion System 1 Recalled by...
The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart FRx 861304 Automated External Defibrillator Manufactured...
The Issue: Philips determined that it is important to clarify information in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System 1 base 220/240V The Terumo Advanced Perfusion System 1 Recalled by...
The Issue: Terumo Cardiovascular Systems sent a Safety Advisory (AA-2010-007-C) on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap S4 Element 4.5mm Polyaxial Screws (ST240T Recalled by Aesculap...
The Issue: There is a possibility that the screw channel that holds the rod in place...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Myocardial Heart Wires Intended for temporary atrial and ventricular pacing...
The Issue: Oscor, Inc. in Palm Harbor, FL is recalling myocardial heart wires, models...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens ADVIA Centaur Multi-Diluent 1 - Used for automated dilutions...
The Issue: Decrease in onboard dilution recovery when using Multi-Diluent 1 that has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Essenta DR Recalled by Philips Healthcare Inc. Due to Essenta DR...
The Issue: Essenta DR C-Arm may fall
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Folate Calibrators Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Access Folate WHO Calibrators Recalled by Beckman Coulter Inc. Due to...
The Issue: Beckman Coulter is recalling the Access Folate Calibrators because it may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capintec Captus 3000 Thyroid Uptake System Nuclear uptake probe intended...
The Issue: Customers who received a Capintec Captus 3000 Thyroid Uptake System with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Spine EXPEDIUM Offset Torque Wrench Product Code 2797-29-510 The...
The Issue: A component within the handle of the Expedium Offset Torque Wrench is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cisco brand HealthPresence Recalled by Cisco Systems Inc Due to Software...
The Issue: Software anomaly may result in incorrect values and interpretations. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VersaTREK Windows Software Recalled by Trek Diagnostic Systems Due to Review...
The Issue: Review of instrument software databases and investigation of two customer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TAUT Recalled by Teleflex Medical Due to Product is missing the label on the...
The Issue: Product is missing the label on the internal packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Visual-ICE¿ Cryoablation System Recalled by Galil Medical, Inc. Due to Galil...
The Issue: Galil Medical is recalling a number of Visual Ice Cryoablation Systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESCAPE Monitor B850 Product Usage: The CARESCAPE TM Monitor B850 Recalled...
The Issue: GE Healthcare become aware of 4 potential issues associated with the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laserworld RGB & Piko Nano RGB Models All models are Recalled by Laserworld...
The Issue: A potential lack of certification, and/or missing laser certification, laser...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cliniqa Liquid QCTM Cardiac Marker Control for i-STAT Level 1 Recalled by...
The Issue: Abbott Point of Care (APOC) has determined that for the Cliniqa Liquid QC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00-4309-028-01 - Trabecular Metal Reverse Shoulder Liner 40mm 65¿ Neck...
The Issue: Lot specific Trabecular Metal (TM) Reverse Shoulder Liner Impactors are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.