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 261280 of 30,921 recalls

Medical DeviceDecember 19, 2025· Tyber Medical

Recalled Item: Brand Name: VOLT" Wrist Treatment System Product Name: 2.4/2.7 2Column...

The Issue: The supplier manufactured anatomical left plates with an incorrect thread...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: VANTAGE GALAN 3T Model MRT-3020/MEXL-3020 Recalled by Canon Medical System,...

The Issue: There is a potential for formation of ice occurring in the venting system of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· ICU Medical Inc.

Recalled Item: Pulsator Arterial Blood Sampling Kit Recalled by ICU Medical Inc. Due to...

The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· Canon Medical System, USA, INC.

Recalled Item: VANTAGE TITAN 3T Model MRT-3010/MEXL-3010 Recalled by Canon Medical System,...

The Issue: There is a potential for formation of ice occurring in the venting system of...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2025· ICU Medical Inc.

Recalled Item: Portex Spinal Tray Recalled by ICU Medical Inc. Due to Affected lots of...

The Issue: Affected lots of syringes may have a crack on the syringe collar, which may...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Vascutek, Ltd.

Recalled Item: Gelsoft Plus Recalled by Vascutek, Ltd. Due to Gelatin sealed woven...

The Issue: Gelatin sealed woven polyester prostheses devices, designed for vascular...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2025· Community Products, LLC

Recalled Item: Rifton Equipment Recalled by Community Products, LLC Due to Potential for...

The Issue: Potential for fraying on the body support strap.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: AlternatiV+ Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Genesis Push-In Suture Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Fixone Biocomposite Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Fixone Hybrid Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Genesis Knotless Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: AlternatiV+ Max Knotless Anchor Recalled by Aju Pharm Co., Ltd. Due to...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Genesis Dual Thread Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2025· Aju Pharm Co., Ltd.

Recalled Item: Genesis Screw-In Anchor Recalled by Aju Pharm Co., Ltd. Due to Reports of...

The Issue: Reports of device failure, including anchor breakage, anchor bending, anchor...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Convenience Kits 1. 25GA Convenience Kit - FNX VS0644.25-FNX 2. Recalled by...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical 1. 23GA Laser Probe Curved Cat No. VS0120.23 Recalled by...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Vortex Surgical I2 Injection Kit Recalled by Vortex Surgical Inc. Due to...

The Issue: There may be voids located in the seal of Tyvek pouches associated with...

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

Class II — Potential Health HazardOngoing