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. 2,884 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,884 in last 12 months

Showing 46614680 of 30,921 recalls

Medical DeviceMarch 5, 2024· Quidel Corporation

Recalled Item: QUIDEL InflammaDry MMP-9 Test Recalled by Quidel Corporation Due to There...

The Issue: There are two windows on the test device, the control line window and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2024· Baxter Healthcare Corporation

Recalled Item: Hill-Rom PRO+ 36" MRS Surface Recalled by Baxter Healthcare Corporation Due...

The Issue: Inconsistencies were identified with service records associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2024· Unomedical A/S

Recalled Item: Neria Soft Infusion Set Recalled by Unomedical A/S Due to Specific lots of...

The Issue: Specific lots of Neria Soft Infusion Sets, which have been shipped into the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 5, 2024· Beckman Coulter, Inc.

Recalled Item: DxI 9000 Access Immunoassay Analyzer Recalled by Beckman Coulter, Inc. Due...

The Issue: Beckman Coulter manufacturing discovered cracks around a threaded insert on...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Avanos Medical, Inc.

Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...

The Issue: The expiration date was not printed on the outer shipping label, leading to...

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

Class III — Low RiskOngoing
Medical DeviceMarch 4, 2024· Avanos Medical, Inc.

Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...

The Issue: The expiration date was not printed on the outer shipping label, leading to...

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

Class III — Low RiskOngoing
Medical DeviceMarch 4, 2024· Avanos Medical, Inc.

Recalled Item: NEOMED* Pharmacy Syringes - Nonsterile (Non ENFit) with below product...

The Issue: The expiration date was not printed on the outer shipping label, leading to...

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

Class III — Low RiskOngoing
Medical DeviceMarch 4, 2024· Abbott GmbH

Recalled Item: Alinity i Anti-HCV Reagent Kit Recalled by Abbott GmbH Due to Customer...

The Issue: Customer complaints were received regarding falsely elevated results for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Ion Beam Applications S.A.

Recalled Item: IBA Proton Therapy System - PROTEUS 235 Recalled by Ion Beam Applications...

The Issue: There is a risk of mistreatment as irradiation is not prevented when some...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· X-NAV Technologies, LLC

Recalled Item: X-Guide Handpiece Adaptor Sleeve 3 Recalled by X-NAV Technologies, LLC Due...

The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Abbott GmbH

Recalled Item: ARCHITECT Anti-HCV Reagent Kit Recalled by Abbott GmbH Due to Customer...

The Issue: Customer complaints were received regarding falsely elevated results for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· X-NAV Technologies, LLC

Recalled Item: X-Guide Handpiece Adaptor Sleeve 1 Recalled by X-NAV Technologies, LLC Due...

The Issue: The Handpiece Adaptor may have a manufacturing defect causing incorrect...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 4, 2024· Qiagen Sciences LLC

Recalled Item: EZ2 Connect MDx-IVD Designed to perform automated isolation and purification...

The Issue: Insufficient welding leads to the heater cable becoming brittle and present...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Thoratec Corp.

Recalled Item: Thoratec HeartMate 3 Recalled by Thoratec Corp. Due to Potential for a leak...

The Issue: Potential for a leak path at the seal interface between the left ventricle...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· Alere San Diego, Inc.

Recalled Item: Abbott Cholestech LDX Battery Kit Recalled by Alere San Diego, Inc. Due to...

The Issue: There is a potential that the Cholestech LDX battery (an external battery...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Thoratec Corp.

Recalled Item: Thoratec HeartMate 3 Recalled by Thoratec Corp. Due to Potential for a leak...

The Issue: Potential for a leak path at the seal interface between the left ventricle...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Peel-Away Introducer - Intended for the percutaneous introduction of balloon...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Dilator - Intended to be used for dilating puncture sites Recalled by Cook...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Entuit Secure Adjustable Gastrointestinal Suture Anchor Set - Intended for...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 1, 2024· Cook Incorporated

Recalled Item: Yueh Centesis Disposable Catheter Needle - Intended for use in Recalled by...

The Issue: Packaging may have low seal strength and not meet peel strength...

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

Class II — Potential Health HazardOngoing