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 2728127300 of 30,921 recalls

Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 29ga Oshima Dual Chandelier Recalled by Synergetics Inc Due to Faulty seals...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals on the...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Becton Dickinson & Co.

Recalled Item: BD BACTEC FX- Top Unit instrument Recalled by Becton Dickinson & Co. Due to...

The Issue: Improperly functioning component of a diagnostic medical device may cause...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 25ga Aspirating Endo Illuminator Recalled by Synergetics Inc Due to Faulty...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Chow Illuminated Pick Recalled by Synergetics Inc Due to Faulty seals...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Straight Fixed Extended Illuminated Laser Probe Recalled by Synergetics...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Wide Field Corona Endo Illuminator Recalled by Synergetics Inc Due to...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Stiff 25ga Chow Illuminated Pick (Dull) Recalled by Synergetics Inc Due to...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: 23ga Aspirating Endo Illuminator Recalled by Synergetics Inc Due to Faulty...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Stiff 25ga Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Wide Field Endo Illuminator Recalled by Synergetics Inc Due to Faulty seals...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Two-Port Vitrectomy (TPV (tm)) Wide Field High Flow End Irrigator Recalled...

The Issue: Faulty seals on the outer pouch of various, double-pouched, single-use,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 9, 2013· Gambro Renal Products, Incorporated

Recalled Item: Gambro Cartridge Blood Set Recalled by Gambro Renal Products, Incorporated...

The Issue: Occluded heparin tubing events preventing anticoagulation dosing on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2013· HeartWare Inc

Recalled Item: Heartware HVAD Pump Implant Kit (Heartware Ventricular Assist Device)...

The Issue: The housing to the Pump's driveline connector became partially or fully...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 6, 2013· Bard Access Systems

Recalled Item: MRI Low Profile Single Lumen port with Open-Ended 6.6Fr Silicone Recalled by...

The Issue: Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2013· Stryker Instruments Div. of Stryker Corporation

Recalled Item: Stryker Color Cuff Recalled by Stryker Instruments Div. of Stryker...

The Issue: The Color Cuff¿ Sterile Disposable Tourniquet Cuffs with Quick-Connect...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2013· Bard Access Systems

Recalled Item: Titanium Single Lumen Low-Profile port Recalled by Bard Access Systems Due...

The Issue: Bard Access Systems is recalling various Low Profile Port with 6.6 Fr Single...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2013· Merit Medical Systems, Inc.

Recalled Item: Catheter Recalled by Merit Medical Systems, Inc. Due to Merit Medical...

The Issue: Merit Medical Systems, Inc. is conducting a recall for 3 lots of Maestro...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 6, 2013· Lab Vision Corporation

Recalled Item: Estrogen Receptor AB-11 (Clone ID5) Mouse Monoclonal Antibody 1 mk Recalled...

The Issue: Reports that the product is not performing as expected. In house testing...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 5, 2013· Philips Medical Systems, Inc.

Recalled Item: Philips Essenta DR Recalled by Philips Medical Systems, Inc. Due to X-ray...

The Issue: X-ray system C-arm casting may loosen and fall

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

Class II — Potential Health HazardOngoing