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 2726127280 of 30,921 recalls

Medical DeviceDecember 9, 2013· Synergetics Inc

Recalled Item: Standard tubing set 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· Synergetics Inc

Recalled Item: 23ga Endo Illuminator (Eckardt Trocar Compatible) 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: 25ga Awh Chandelier 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· Synergetics Inc

Recalled Item: 27ga ONE-STEP (tm) Awh/Tano Vivid Chandelier Recalled by Synergetics Inc Due...

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: Vivid (tm) 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: 25ga Mid-Field 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· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT & Brilliance iCT SP Computed Tomography X-Ray Systems...

The Issue: Patient images exhibited ring artifacts.

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 Awh Chandelier 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· Synergetics Inc

Recalled Item: "The Corona" Shielded Wide Field Endo Illuminator 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: Chandelier Infusion Cannula 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· Aesculap, Inc.

Recalled Item: Aesculap Hi-Line XXS handpiece Hi-Line XXS handpieces are used with Recalled...

The Issue: Certain lots of the Aesculap Hi Line XXS handpiece (part # GB790R) were...

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

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

Recalled Item: 27ga ONE-STEP (tm) 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 Wide Field 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: 23ga Chandelier Infusion Cannula 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 Mid-Field 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: 25ga 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 40 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 Awh Vivid Chandelier Recalled by Synergetics Inc Due to Faulty seals on...

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: 25ga 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· ArthroCare Medical Corporation

Recalled Item: Arthrocare SPORTS MEDICINE Recalled by ArthroCare Medical Corporation Due to...

The Issue: A sharp edge on the cannulated tip of the device may damage or cut a suture.

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

Class II — Potential Health HazardOngoing