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 2970129720 of 30,923 recalls

Medical DeviceSeptember 20, 2012· Terumo Cardiovascular Systems Corporation

Recalled Item: Terumo Advanced Perfusion System 1 Flow Module indicated for use Recalled by...

The Issue: Terumo Cardiovascular Systems (CVS) received one report of a flow module for...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Captiva Spine, Inc

Recalled Item: CapLOX II Final Torque Driver Recalled by Captiva Spine, Inc Due to Captiva...

The Issue: Captiva Spine recalled their CapLOX II Final Torque Driver, Indicator due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Sorin Group USA, Inc.

Recalled Item: SCP Pump Control Panel Recalled by Sorin Group USA, Inc. Due to Sorin Group...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Zimmer, Inc.

Recalled Item: The Trilogy Acetabular System Shell with Cluster Holes Porous 56 Recalled by...

The Issue: Zimmer Trilogy¿ Acetabular System Shell with Cluster Holes, Porous,56 MM...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Horiba Instruments, Inc dba Horiba Medical

Recalled Item: ABX PENTRA ML Recalled by Horiba Instruments, Inc dba Horiba Medical Due to...

The Issue: Horiba Medical is recalling ABX PENTRA ML because they have confirmed an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Medline Industries Inc

Recalled Item: Medline Total Knee CDS Recalled by Medline Industries Inc Due to The Back...

The Issue: The Back Table Cover component in the custom pack was placed in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Zimmer, Inc.

Recalled Item: The TM Ardis Interbody System Inserter Stainless Steel Recalled by Zimmer,...

The Issue: Zimmer Spine is has received complaints of difficulty in turning the implant...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 20, 2012· Advanced Sterilization Products

Recalled Item: STERRAD NX Cassettes Recalled by Advanced Sterilization Products Due to...

The Issue: Advanced Sterilization Products is recalling three lots of STERRAD NX System...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Cure Medical LLC

Recalled Item: Male Recalled by Cure Medical LLC Due to The firm initiated the product...

The Issue: The firm initiated the product recall because labeling on some of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Trumpf Medical Systems, Inc.

Recalled Item: Helion and Xenion surgical lights Recalled by Trumpf Medical Systems, Inc....

The Issue: Incidents regarding fractures of the front joint of the spring arm have been...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: S5 Mast Roller Pump 85 Recalled by Sorin Group USA, Inc. Due to Sorin Group...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: S5 Double Roller Pump 85 Recalled by Sorin Group USA, Inc. Due to Sorin...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: S5 Mast Roller Pump 150 Recalled by Sorin Group USA, Inc. Due to Sorin Group...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: Sorin C5 Perfusion System Recalled by Sorin Group USA, Inc. Due to Sorin...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2012· Sorin Group USA, Inc.

Recalled Item: S5 Single Roller Pump 150 Recalled by Sorin Group USA, Inc. Due to Sorin...

The Issue: Sorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental CS 2200 X-ray system Product Usage: The expected Recalled...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Elekta, Inc.

Recalled Item: MOSAIQ MOSAIQ is an image-enabled electronic medical record system (EMR)...

The Issue: A patient was seriously mistreated after a user made and saved an...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental Kodak 2200 Intraoral X-ray system Product Usage: The...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Trophy Sas

Recalled Item: CareStream Dental CS 2100 X-ray system Product Usage: The expected Recalled...

The Issue: There have been approximately 2% of the x-ray generators manufactured...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2012· Philips Medical Systems (Cleveland) Inc

Recalled Item: Mx8000 IDT Whole Body Computed Tomography X-ray system Distributed by...

The Issue: The low contrast pins in the Image Quality (IQ) phantom deteriorates over...

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

Class II — Potential Health HazardOngoing