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. 1,016 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
1,016 in last 12 months

Showing 40601–40620 of 55,713 recalls

Medical DeviceAugust 10, 2015· Biomet 3i, LLC

Recalled Item: Biomet 3i Narrow Right Angle Square Driver Tip. Driver tips Recalled by...

The Issue: RASQ3N, a square, abutment screw driver tip has been labeled and distributed...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 10, 2015· Biomet 3i, LLC

Recalled Item: Biomet 3i Narrow Right Angle Large Driver Tip (Hexed). Driver Recalled by...

The Issue: The RASH3N, a hexed, abutment screw driver tip has been labeled and...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Fundus Grasper Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Medium -Large Clip Applier Recalled by Intuitive Surgical, Inc. Due to In...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Cadiere Forceps Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Fenestrated Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Maryland Dissector Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Curved Needle Driver Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Crocodile Grasper Recalled by Intuitive Surgical, Inc. Due to In certain...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 8, 2015· Intuitive Surgical, Inc.

Recalled Item: Maryland Bipolar Forceps Recalled by Intuitive Surgical, Inc. Due to In...

The Issue: In certain circumstances involving select da Vinci Si Single-Site...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· International Biophysics Corp.

Recalled Item: IBC Suction Wand Catalog Number 1990S Product Usage: The IBC Recalled by...

The Issue: It was discovered that the heat seal placed onto sterile pouches may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· Carestream Health Inc

Recalled Item: CARESTREAM DRX-EVOLUTION X-Ray System Product Usage: The device is a...

The Issue: Software defect that impacts image alignment when using the automatic...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· Terumo Cardiovascular Systems Corporation

Recalled Item: CDI 500 Blood Parameter Monitoring System. Provides continuous Recalled by...

The Issue: Inaccuracies in SvO2, temperature, pH, pCO2, pO2, Hematocrit, and Potassium...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· International Biophysics Corp.

Recalled Item: IBC Vascular Loop Catalog Number CH111 Recalled by International Biophysics...

The Issue: It was discovered that the heat seal placed onto sterile pouches may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2015· International Biophysics Corp.

Recalled Item: IBC Aortic Punch Catalog Numbers APM40 Recalled by International Biophysics...

The Issue: It was discovered that the heat seal placed onto sterile pouches may not...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Mahurkar Acute Dual Lumen Catheter Tray Recalled by Covidien LLC Due to...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: MAHURKAR 12Fr High Pressure Triple Lumen Acute Dialysis Catheter Recalled by...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Tornier, Inc

Recalled Item: Salto Talaris Tibial Guide Recalled by Tornier, Inc Due to Tornier has...

The Issue: Tornier has initiated a voluntary recall for the Salto Talaris Tibial Guide...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 6, 2015· Covidien LLC

Recalled Item: Monoject 0.9% Saline Flush Prefill Double Pouch Item Code: 8881570129...

The Issue: Sterility may be compromised

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

Class II — Potential Health HazardOngoing