Product Recalls in Texas

Product recalls affecting Texas — including food, drugs, consumer products, medical devices, and vehicles distributed to Texas. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,680 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,680 in last 12 months

Showing 2596125980 of 30,921 recalls

Medical DeviceJuly 3, 2014· Intelerad Medical Systems

Recalled Item: IntelePACS software versions 3-8-1 to 4-9-1 Recalled by Intelerad Medical...

The Issue: In specific situation a partially truncated file may be written to the...

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 Unitized Catheter and Accessories...

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¿ 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 with SIPHONGUARD¿ Device Recalled by...

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· 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 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· Spacelabs Healthcare Inc

Recalled Item: ARIATELE TELEMETRY TRANSMITTER Recalled by Spacelabs Healthcare Inc Due to...

The Issue: The transmitter display and the Telemetry Central Station display may show a...

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: 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· 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: 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· 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· 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· Teleflex Medical

Recalled Item: RUSCH Recalled by Teleflex Medical Due to There is a possibility the handle...

The Issue: There is a possibility the handle of the laryngoscope may heat up and melt...

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

Class II — Potential Health HazardOngoing