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.

56,506 total recalls
2,839 in last 12 months

Showing 2702127040 of 30,923 recalls

Medical DeviceJanuary 27, 2014· Synthes, Inc.

Recalled Item: Synthes Matrix Mandible Short Threaded Drill Guide intended for oral...

The Issue: One lot of Matrix Mandible Short Threaded Drill Guides (part No. 03.503.043)...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Hologic, Inc

Recalled Item: NovaSure Impedance Controlled Endometrial Ablation System Radiofrequency...

The Issue: NovaSure Radiofrequency Control Units may not meet a requirement of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Clarity Medical Systems Inc

Recalled Item: RetCam 3 Recalled by Clarity Medical Systems Inc Due to Software anomaly for...

The Issue: Software anomaly for RetCam 3, RetCam Shuttle and RetCam Portable with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Philips Medical Systems, Inc.

Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model: 861290 The HeartStart...

The Issue: HeartStart XL+ battery charge time to 100% capacity at 35¿C (95¿F) is...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Carestream Health Inc.

Recalled Item: Model Kodak 2100 Intraoral X-Ray System Recalled by Carestream Health Inc....

The Issue: Carestream received problem reports relating to apparent early failure of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling

The Issue: Mislabeled product.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Carestream Health Inc.

Recalled Item: Model Kodak 2200 Intraoral X-Ray System Recalled by Carestream Health Inc....

The Issue: Carestream received problem reports relating to apparent early failure of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Hospira Inc.

Recalled Item: Plum XL3 Multi line Infusion System Recalled by Hospira Inc. Due to There is...

The Issue: There is the potential for the door roller assembly on the Plum LifeCare...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Hospira Inc.

Recalled Item: LifeCare 5000 Pump (Plum 1.6) infusion pump Recalled by Hospira Inc. Due to...

The Issue: There is the potential for the door roller assembly on the Plum LifeCare...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 24, 2014· Hospira Inc.

Recalled Item: Plum XL Recalled by Hospira Inc. Due to There is the potential for the door...

The Issue: There is the potential for the door roller assembly on the Plum LifeCare...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 23, 2014· Atricure Inc

Recalled Item: Reusable Clip Applier Manufactured by AtriCure Recalled by Atricure Inc Due...

The Issue: The firm was notified by a customer of a cracked spring in the handle of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2014· Integra LifeSciences Corp.

Recalled Item: Malibu Polyaxial Screwdriver Recalled by Integra LifeSciences Corp. Due to...

The Issue: Integra LifeSciences has identified through an investigation of complaints...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 22, 2014· CareFusion 303, Inc.

Recalled Item: SmartSite Needleless Connector Recalled by CareFusion 303, Inc. Due to...

The Issue: CareFusion is recalling the SmartSite Needlefree Connector, model number...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2014· Golden Technologies, Inc.

Recalled Item: Buzzaround XL scooters' Product Usage: mobility Recalled by Golden...

The Issue: Buzzaround XL scooters' front to rear lockup can become unintentionally...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 21, 2014· Dako North America Inc.

Recalled Item: Product Name: HER2 CISH pharmDx Kit Catalog/Model number: SK109 Recalled by...

The Issue: Dako has initiated a recall of HER2 CISH pharmDxTM Kit because weak red...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Precision 500D and Proteus XR/a equipped with Wireless...

The Issue: GE Healthcare has recently become aware of a software issue associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2014· Edwards Lifesciences, LLC

Recalled Item: Crimper Model 9100CR26 The Crimper is indicated for use in Recalled by...

The Issue: Edwards Lifesciences is recalling two lot numbers of the 26mm transcatheter...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 20, 2014· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA Multical. ABX PENTRA N Control. ABX PENTRA P Recalled by Horiba...

The Issue: HORIBA Medical is informing all ABX PENTRA MultiCal, N Control, and P...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2014· Medical Information Technology, Inc.

Recalled Item: MEDITECH Microbiology - Calculator/data processing module Recalled by...

The Issue: Potential for patient results being removed from LAB/EMR.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2014· CareFusion 303, Inc.

Recalled Item: Trifurcated Extension Set Recalled by CareFusion 303, Inc. Due to CareFusion...

The Issue: CareFusion is recalling the Trifurcated Extension Set, models ME 1224 and MP...

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

Class II — Potential Health HazardOngoing