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. 2,723 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,723 in last 12 months

Showing 1728117300 of 30,921 recalls

Medical DeviceMarch 28, 2018· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation Radiation Therapy Treatment Planning System Recalled by RAYSEARCH...

The Issue: The dose calculation accuracy may in some situations be less than expected....

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Draegar Medical Systems, Inc.

Recalled Item: Infinity Acute Care System (lACS) Monitoring Solution Recalled by Draegar...

The Issue: Software anomaly resulting in the loss of patient settings and stored...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 28, 2018· Zimmer Biomet, Inc.

Recalled Item: Gentle Threads Recalled by Zimmer Biomet, Inc. Due to Specific lots of the...

The Issue: Specific lots of the device were overexposed during EtO sterilization. This...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Trilliant Surgical Ltd.

Recalled Item: Ratcheting Cannulated Driver Handle Recalled by Trilliant Surgical Ltd. Due...

The Issue: Firm is voluntarily recalling cannulated driver handles (210-00-003 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Trilliant Surgical Ltd.

Recalled Item: Cannulated Driver Handle Recalled by Trilliant Surgical Ltd. Due to Firm is...

The Issue: Firm is voluntarily recalling cannulated driver handles (210-00-003 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Urea Nitrogen Reagent (material number 10309051) for use...

The Issue: Urea Nitrogen reagent kit demonstrated an increased incidence of Calibration...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.Via VB20A model 1049610 Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Functionality in the report sections "Findings Information" and "Summary of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2018· Teleflex Medical Europe Ltd

Recalled Item: Teleflex MEDICAL HUDSON RCI One Way Valve w. Capped Monitoring Port Recalled...

The Issue: These one-way valves may disconnect at the joint between the two components...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Ethicon Endo-Surgery Inc

Recalled Item: 5mm Endopath Xcel with Optiview Technology Recalled by Ethicon Endo-Surgery...

The Issue: Use of the product with insufficient lubrication may prolong surgery due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Beckman Coulter Inc.

Recalled Item: BECKMAN COULTER MicroScan MICroSTREP Plus Panel Recalled by Beckman Coulter...

The Issue: Beckman Coulter has received customer complaints of lowered minimum...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 26, 2018· Tornier, Inc

Recalled Item: AEQUALIS HUMERAL NAIL DRILL BIT Recalled by Tornier, Inc Due to Drill bit...

The Issue: Drill bit tips without new BargerGard tip protector may puncture through...

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

Class II — Potential Health HazardOngoing