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.

56,506 total recalls
2,851 in last 12 months

Showing 2442124440 of 30,923 recalls

Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - Fluted Barrel Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 2.3MM Fluted Matchstick Recalled by The Anspach Effort, Inc. Due...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 3MM Fluted Ball Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Philips Ultrasound, Inc.

Recalled Item: EPIQ 5 Ultrasound System with Pediatric Cardiology option Recalled by...

The Issue: When Epiq 5 Ultrasound System, WITH the Pediatric Cardiology option, is set...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Philips Ultrasound, Inc.

Recalled Item: EPIQ 7 Ultrasound System with Pediatric Cardiology option Recalled by...

The Issue: When Epiq 7 Ultrasound System, WITH the Pediatric Cardiology option, is set...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Medtronic Neuromodulation

Recalled Item: Medtronic SynchroMed II Implantable Infusion Pumps Recalled by Medtronic...

The Issue: Medtronic is conducting a recall of a specific subset of Model 8637-20 and...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Alphatec Spine, Inc.

Recalled Item: 4.0mm Variable Angle Recalled by Alphatec Spine, Inc. Due to Mislabeling

The Issue: During a field audit it was discovered by an employee that a 16mm Trestle...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2015· Coloplast Manufacturing US, LLC

Recalled Item: Genesis Malleable Penile Prosthesis Recalled by Coloplast Manufacturing US,...

The Issue: Several lots of the 9.5 mm Genesis Malleable Penile Prosthesis were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2015· Spinal Elements, Inc

Recalled Item: Spinal Elements 5.5 x 45MM Mercury lordosed rod. A component Recalled by...

The Issue: Some rods may not meet the appropriate traceability requirements including...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
Medical DeviceApril 9, 2015· Synthes, Inc.

Recalled Item: TFN-ADVANCED Proximal Femoral Nailing System (TFNA) Recalled by Synthes,...

The Issue: TFNA nails from certain lots were assembled with a locking mechanism too...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2015· Bard Peripheral Vascular Inc

Recalled Item: BARD MAX-CORE Disposable Core Biopsy Instrument Gauge x Length 18g Recalled...

The Issue: The firm is recalling Bard MAX-CORE Disposable Core Biopsy Instrument due to...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 9, 2015· BTE Technologies, Inc.

Recalled Item: Primus (THE BTE WS30) Recalled by BTE Technologies, Inc. Due to On the...

The Issue: On the Primus that includes the optional Chop / Lift Bar, there is a remote...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 8, 2015· Baxter Corporation Englewood

Recalled Item: ABACUS SE (Single-Workstation Edition) and ABACUS ME (Multi-Workstation...

The Issue: Baxter Corporation is conducting a field action for the ABACUS SE and ME...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2015· Catheter Research, Inc

Recalled Item: HSG Trays/HS 5F Catheter Combo Recalled by Catheter Research, Inc Due to...

The Issue: HSG Trays and Catheters were mislabeled. Trays with the flexible HS catheter...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: Assay Data Disk (ADD) Recalled by Ortho-Clinical Diagnostics Due to Software...

The Issue: Software anomaly regarding urine samples that require acidified...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· GA Industries

Recalled Item: Logicon Caries Detector Product Usage: Analyze inter-proximal tooth surfaces...

The Issue: GA Industries is recalling the Logicon Caries Detector, version 5.0, for...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5 Recalled by Ortho-Clinical Diagnostics Due to Software anomaly...

The Issue: Software anomaly regarding urine samples that require acidified...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 4600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly allows testing of multiple assays using a single urine...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2015· Ortho-Clinical Diagnostics

Recalled Item: VITROS 5600 Chemistry System Recalled by Ortho-Clinical Diagnostics Due to...

The Issue: Software anomaly allows testing of multiple assays using a single urine...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceApril 3, 2015· Carefusion 211 Inc dba Carefusion

Recalled Item: CareFusion AVEA ventilator Recalled by Carefusion 211 Inc dba Carefusion Due...

The Issue: A pressure transducer failure can develop, activating a false Extended High...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing