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 2506125080 of 30,921 recalls

Medical DeviceDecember 8, 2014· Baxter Healthcare Corp.

Recalled Item: Baxter Integrated APD Set with Cassette 3-Prong Recalled by Baxter...

The Issue: Baxter is issuing a recall for one lot of Integrated Automated Peritoneal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2014· Radiometer America Inc

Recalled Item: ABL90 FLEX analyzer Recalled by Radiometer America Inc Due to The ABL90...

The Issue: The ABL90 analyzer does not always use the most recent calibration data to...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 8, 2014· Philips Medical Systems (Cleveland) Inc

Recalled Item: Various Brilliance and Ingenuity Computed Tomography X-ray systems Recalled...

The Issue: Improper assembly of the vertical motor/brake system may lead to uncommanded...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2014· Invacare Corporation

Recalled Item: G- Series Beds Recalled by Invacare Corporation Due to Invacare identified...

The Issue: Invacare identified that the rail mounting bracket on the G29 full length...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2014· Intuitive Surgical, Inc.

Recalled Item: IS3000 Vision Side Cart (VSC) used in conjunction with the Recalled by...

The Issue: Intuitive Surgical is initiating a voluntary correction related to da Vinci...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2014· Alere San Diego, Inc.

Recalled Item: INRatio 2 Monitors - 0200431 Alere INRatio 2 PT/INR Professional Recalled by...

The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 5, 2014· Alere San Diego, Inc.

Recalled Item: Alere INRatio PT/INR Test Strips Recalled by Alere San Diego, Inc. Due to In...

The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 5, 2014· Alere San Diego, Inc.

Recalled Item: INRatio Monitors - 0100004 Alere INRatio PT/INR System Professional -...

The Issue: In certain cases, an INRatio PT/INR Monitor system may provide an INR result...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 4, 2014· Zimmer Manufacturing B.V.

Recalled Item: Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD The Recalled by Zimmer...

The Issue: Zimmer received a single complaint wherein a Trilogy® Fiber Metal...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle- Model...

The Issue: There is the potential for a breach in the inner or outer packaging pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Baxter Corporation Englewood

Recalled Item: Self-Righting Luer Lock Tip Cap Recalled by Baxter Corporation Englewood Due...

The Issue: Baxter Corporation initiated a recall of two lots of Self-Righting Luer Lock...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Orthovita, Inc., dBA Stryker Orthobiologics.

Recalled Item: Stryker Orthobiologics Imbibe Bone Marrow Aspiration Needle Recalled by...

The Issue: There is the potential for a breach in the inner or outer packaging pouches...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Hansen Medical Inc

Recalled Item: Sensei X Robotic Catheter System Recalled by Hansen Medical Inc Due to The...

The Issue: The Set Up Joint subassembly of the Sensei X Robotic Catheter System may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 4, 2014· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: DBX Mix Recalled by Musculoskeletal Transplant Foundation, Inc. Due to The...

The Issue: The seal on the DBX Mix outer PETG/Aclar tray with foil lid packaging for...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Leonhard Lang Gmbh

Recalled Item: GE Healthcare Pediatric Direct-Wired Disposable Defibrillation/Pacing...

The Issue: The firm discovered that during the use of these defibrillation electrodes a...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: Cable remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: (R)IR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUPITER / TS7500 Recalled by Trumpf Medical Systems, Inc....

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IIR remote control JUPITER Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 3, 2014· Trumpf Medical Systems, Inc.

Recalled Item: IR remote control JUC Recalled by Trumpf Medical Systems, Inc. Due to...

The Issue: Complaints have been reported of unintended movement occurring during...

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

Class II — Potential Health HazardOngoing