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 2592125940 of 30,923 recalls

Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Recalled by Codman &...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve Only Recalled by Codman & Shurtleff, Inc. Due...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 3, 2014· Codman & Shurtleff, Inc.

Recalled Item: Codman Certas - In Line Valve with SIPHONGUARD¿ Device Recalled by Codman &...

The Issue: To clarify the CODMAN CERTAS Valve virtual off (setting 8) pressure...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2014· Mentor Texas, LP.

Recalled Item: EN MENTOR Round High Profile Single Use Saline Breast Implant Recalled by...

The Issue: The device labeling is stamped with 330cc and the device is actually 380cc...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2014· Smith & Nephew, Inc.

Recalled Item: TRIGEN(R) INTERTAN(TM) 10MM X 18 CM NAIL Recalled by Smith & Nephew, Inc....

The Issue: There was an error in manufacturing which resulted in the proximal lag screw...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 2, 2014· Hospira Inc.

Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....

The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...

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

Class I — Serious Health HazardOngoing
Medical DeviceJuly 1, 2014· PerkinElmer Health Sciences, Inc.

Recalled Item: Panthera-Puncher 9 . Panthera-Puncher 9 is a sample transfer instrument...

The Issue: Risk of incorrect results from samples prepared with Panthera-Puncher 9

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2014· Zimmer, Inc.

Recalled Item: PERSONA (TM) The Personalized Knee System Tibial General Instrument Tray...

The Issue: The firm discovered that the current Personal Tibial/General Fixed Bracket...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2014· Zimmer, Inc.

Recalled Item: Moore Hip Prosthesis Long Fenestrated Stem 38 mm (1-1/2 Inch) Recalled by...

The Issue: Zimmer is initiating a voluntary recall of 20 production lots of Moore Hip...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2014· Zimmer, Inc.

Recalled Item: PERSONA (TM) The Personalized Knee System Tibial General Instrument Tray...

The Issue: The firm discovered that the current Personal Tibial/General Fixed Bracket...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 1, 2014· Ansar Group, Inc. Dba Ansar Medical Technologies, Inc

Recalled Item: Blood pressure (BP) circuit of the ANSAR ANX-3.0 Autonomic Monitor Recalled...

The Issue: The blood pressure (BP) circuit occasionally fails to inflate the blood...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Steris Corporation

Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Product Usage: Usage: The...

The Issue: STERIS has identified that deformation of the washers door handle pin may...

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

Class III — Low RiskOngoing
Medical DeviceJune 30, 2014· Invivo Corporation

Recalled Item: Philips IP5 Information Portal The Expression Information Portal (Model IP5)...

The Issue: The wireless function of the IP5 radio could be interrupted causing loss of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens syngo Imaging XS Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Siemens has become aware of the potential malfunction when using syngo...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 30, 2014· Ra Medical Systems Inc

Recalled Item: PHAROS Excimer Laser Recalled by Ra Medical Systems Inc Due to RA Medical...

The Issue: RA Medical Systems is recalling the PHAROS EX-308 Excimer Laser because...

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

Class II — Potential Health HazardOngoing