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. 2,910 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,910 in last 12 months

Showing 2140 of 55,713 recalls

Medical DeviceFebruary 6, 2026· International Life Sciences

Recalled Item: Artelon FlexBand Plus & 41057 Recalled by International Life Sciences Due to...

The Issue: Augmentation devices failed bacterial endotoxin testing.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 6, 2026· Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha

Recalled Item: Brand Name: Hitachi Proton Beam Therapy System Recalled by Hitachi, Ltd....

The Issue: Software anomaly in the patient positioning system may result in positional...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 6, 2026· Trividia Health, Inc.

Recalled Item: Owner's Booklets and Instructions for Use that are used with Recalled by...

The Issue: The system labeling (user manual and online labeling) did not provide...

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

Class I — Serious Health HazardOngoing
Medical DeviceFebruary 6, 2026· International Life Sciences

Recalled Item: Artelon FLEXBAND TWIST .12 3.85x17mm HEX Anchor (Qty Recalled by...

The Issue: Augmentation devices failed bacterial endotoxin testing.

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

Class II — Potential Health HazardOngoing
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: vancomycin HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: ketamine HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: vancomycin HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: acyclovir sodium Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 5, 2026· Remel, Inc

Recalled Item: Campy CVA Medium 100/PK Recalled by Remel, Inc Due to Customer complaints...

The Issue: Customer complaints report low to no recovery of Campylobacter Jejuni ATCC...

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

Class II — Potential Health HazardOngoing
DrugFebruary 5, 2026· Fresenius Kabi Compounding, LLC

Recalled Item: thiamine HCl Recalled by Fresenius Kabi Compounding, LLC Due to Lack of...

The Issue: Lack of Assurance of Sterility

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 4, 2026· Diagnostica Stago, Inc.

Recalled Item: Brand Name: STA Liatest Free Protein S Product Name: STA Recalled by...

The Issue: The potential of out-of-range results and an underestimation of the free...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2026· Ion Beam Applications S.A.

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

The Issue: It was identified that eh Universal Beam Triggering Interface (UBTI) is...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2026· Exactech, Inc.

Recalled Item: Brand Name: Equinoxe Ergo Product Name: Ergo Modular Impactor Handle...

The Issue: Impactor handle may be missing cross-pin

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 3, 2026· Exactech, Inc.

Recalled Item: Brand Name: Equinoxe Product Name: Equinoxe Core Instrument Kit...

The Issue: Impactor handle may be missing cross-pin

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

Class II — Potential Health HazardOngoing
FoodFebruary 3, 2026· Pure Solutions, Inc.

Recalled Item: Pure Factors Professional Nighttime Sleep Formula and Pure Formulas Sleep...

The Issue: Label declares bovine colostrum but does not declare milk allergen.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceFebruary 2, 2026· B Braun Medical Inc

Recalled Item: Brand Name: B. Braun Product Name: 21GA WINGED INFUSION Recalled by B Braun...

The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 2, 2026· B Braun Medical Inc

Recalled Item: Brand Name: B. Braun Product Name: BBraun Medical 21G X4.4CM Recalled by B...

The Issue: The potential for the needle tip to be dull/blunt, difficult to advance,...

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

Class II — Potential Health HazardOngoing