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. 2,237 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,237 in last 12 months

Showing 58615880 of 30,921 recalls

Medical DeviceSeptember 1, 2023· Onkos Surgical, Inc.

Recalled Item: Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for breach...

The Issue: Potential for breach of Tyvek seals.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Onkos Surgical, Inc.

Recalled Item: Ethos Collar Stem Recalled by Onkos Surgical, Inc. Due to Potential for...

The Issue: Potential for breach of Tyvek seals.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Angel Medical Systems, Inc.

Recalled Item: Brand Name: The Guardian System Product Name: The Guardian Model/Catalog...

The Issue: Device reaching End of Service prematurely.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Onkos Surgical, Inc.

Recalled Item: a. Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for...

The Issue: Potential for breach of Tyvek seals.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Onkos Surgical, Inc.

Recalled Item: Male-Female Midsection with the following sizes and model numbers. a....

The Issue: Potential for breach of Tyvek seals.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Onkos Surgical, Inc.

Recalled Item: Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for breach...

The Issue: Potential for breach of Tyvek seals.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 1, 2023· Onkos Surgical, Inc.

Recalled Item: Segmental Stem Recalled by Onkos Surgical, Inc. Due to Potential for breach...

The Issue: Potential for breach of Tyvek seals.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Pulmonx, Corp.

Recalled Item: Zephyr Endobronchial Valve (EBV) 5.5-LP Recalled by Pulmonx, Corp. Due to...

The Issue: Endobronchial implant devices may have been labeled with a shortened...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Philips North America Llc

Recalled Item: EarlyVue VS30 Vital Signs Monitor Recalled by Philips North America Llc Due...

The Issue: A software issue prevents the monitor from alarming when the high/low...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Access Vascular, Inc

Recalled Item: HydroPICC 5Fr Dual Lumen Maximal Barrier Kit Recalled by Access Vascular,...

The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Access Vascular, Inc

Recalled Item: HydroPICC 5Fr Dual Lumen Recalled by Access Vascular, Inc Due to Specific...

The Issue: Specific lots of the Dual Lumen HydroPICC Kits were provided with the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Philips North America Llc

Recalled Item: EarlyVue VS30 Vitals Monitor Recalled by Philips North America Llc Due to A...

The Issue: A software issue prevents the monitor from alarming when the high/low...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2023· Smith & Nephew Inc

Recalled Item: smith&nephew LEGION OXINUM POSTERIOR STABILIZED NONPOROUS FERMOAL COMPONENT...

The Issue: The firm conducting a recall due to a complaint received indicating that a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· AB Sciex, LLC

Recalled Item: Citrine QTRAP Mass Spectrometer Recalled by AB Sciex, LLC Due to In rare...

The Issue: In rare occasions, the combination of a leak of a highly flammable solvent...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCurity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2023· Stryker Medical Division of Stryker Corporation

Recalled Item: ProCuity bed series Recalled by Stryker Medical Division of Stryker...

The Issue: Patient beds are missing test values for electrical safety tests presenting...

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

Class II — Potential Health HazardOngoing