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 1930119320 of 55,713 recalls

Medical DeviceJuly 20, 2020· Becton Dickinson & Co.

Recalled Item: BD MAX SARS-CoV-2 Reagents Recalled by Becton Dickinson & Co. Due to BD is...

The Issue: BD is experiencing elevated rates of potential false positive results from...

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

Class II — Potential Health HazardOngoing
FoodJuly 18, 2020· Topway Enterprises, Inc

Recalled Item: Tuna cut and packaged in Styrofoam case approximately 19 kg per case...

The Issue: Potential to be contaminated with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 18, 2020· Topway Enterprises, Inc

Recalled Item: Salmon cut and packaged in Styrofoam case approximately 19 kg per case...

The Issue: Potential to be contaminated with Listeria monocytogenes

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 17, 2020· Medtronic Neuromodulation

Recalled Item: Restore Clinician Programmer Application Software Recalled by Medtronic...

The Issue: The original version of the A71100 Restore Clinician Programmer Application...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Materialise N.V.

Recalled Item: Match Point System The Match Point System is intended to Recalled by...

The Issue: The procedure side indicated in the top header of the Shoulder Case Planning...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Cytocell Ltd.

Recalled Item: Cytocell LPH533-A NUP98 Distal Probe Green - Product Usage:The NUP98...

The Issue: A low risk of a false positive result being issued with a laboratory...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS Anti-SARS-CoV-2 IgG Reagent Pack Recalled by Ortho Clinical...

The Issue: The reagent bottles may be swapped within the reagent pack, which may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 17, 2020· Ortho Clinical Diagnostics

Recalled Item: VITROS Anti-SARS-CoV-2 Total Reagent Recalled by Ortho Clinical Diagnostics...

The Issue: The reagent bottles may be swapped within the reagent pack, which may lead...

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

Class II — Potential Health HazardOngoing
FoodJuly 16, 2020· Provident Nutraceutical div. of Ortho Molecular Products Inc

Recalled Item: Dietary supplements Recalled by Provident Nutraceutical div. of Ortho...

The Issue: Various branded dietary supplements may contain undeclared soy.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 16, 2020· J F C International Inc

Recalled Item: Kasugai brand Matcha Ame (Green tea candy) Recalled by J F C International...

The Issue: Undeclared soybean which is contained in lubricant in candy mold.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 16, 2020· Oxford Immunotec

Recalled Item: Model No:T-SPOT.TB8 Recalled by Oxford Immunotec Due to Incorrect expiration...

The Issue: Incorrect expiration date included in test kit labeling and/or in Substrate...

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

Class III — Low RiskOngoing
Medical DeviceJuly 16, 2020· Oxford Immunotec

Recalled Item: Model No:T-SPOT.TB50 Recalled by Oxford Immunotec Due to Incorrect...

The Issue: Incorrect expiration date included in test kit labeling and/or in Substrate...

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

Class III — Low RiskOngoing
Medical DeviceJuly 16, 2020· Brainlab AG

Recalled Item: BRAINLAB Kick 2 Recalled by Brainlab AG Due to Incorrect manufacturer...

The Issue: Incorrect manufacturer calibration

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2020· Brainlab AG

Recalled Item: BRAINLAB Curve Recalled by Brainlab AG Due to Incorrect manufacturer calibration

The Issue: Incorrect manufacturer calibration

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: uEXPLORER PET/CT Diagnostic Imaging System - Product Usage: This system...

The Issue: 1) 1) Potential intermittent issue may cause image data problems, may lead...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2020· Shanghai United Imaging Healthcare Co., Ltd.

Recalled Item: uMI 550 PET/CT Diagnostic Imaging System - Product Usage: This Recalled by...

The Issue: 1) Service function problem may cause false marking of a bad channel...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 16, 2020· Smith & Nephew, Inc.

Recalled Item: Tibial knee prosthesis Recalled by Smith & Nephew, Inc. Due to Due to an...

The Issue: Due to an inconsistency in the raw material process, specific lots may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 15, 2020· OraSure Technologies, Inc.

Recalled Item: Pointts sistema de ellmlnact! Recalled by OraSure Technologies, Inc. Due to...

The Issue: Unit boxes not properly sealed

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

Class III — Low RiskOngoing
Medical DeviceJuly 15, 2020· OraSure Technologies, Inc.

Recalled Item: Personelle OTC Skin Tag Remover Recalled by OraSure Technologies, Inc. Due...

The Issue: Unit boxes not properly sealed

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

Class III — Low RiskOngoing
Medical DeviceJuly 15, 2020· OraSure Technologies, Inc.

Recalled Item: CVS Advanced Wart Remover Kit Recalled by OraSure Technologies, Inc. Due to...

The Issue: Unit boxes not properly sealed

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

Class III — Low RiskOngoing