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 181200 of 30,921 recalls

Medical DeviceJanuary 7, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) CHEST/BREAST-LF Recalled by Medline Industries,...

The Issue: Medline has identified issues related to calibration of the equipment used...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX M150 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX ST150 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: OXIRIS SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a potential...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX ST100 SET US Recalled by VANTIVE US HEALTHCARE LLC Due to There...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· Straumann USA LLC

Recalled Item: WB Impression Post Closed Tray incl. guide screw Recalled by Straumann USA...

The Issue: The mix up of the impression caps provided in the package. The provided...

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

Class III — Low RiskOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX HF1000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRIMSAFLEX M100 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is a...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 6, 2026· VANTIVE US HEALTHCARE LLC

Recalled Item: PRISMAFLEX TPE2000 SET Recalled by VANTIVE US HEALTHCARE LLC Due to There is...

The Issue: There is a potential dislodgement of the Prismaflex Set deaeration chamber...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2026· Medline Industries, LP

Recalled Item: Medline Sterile Saline Wound Wash Recalled by Medline Industries, LP Due to...

The Issue: Medline has identified that the manufacturer of the sterile saline wound...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) TRUNK KIT W/EXPIRATION Recalled by Medline...

The Issue: Medline has identified that the manufacturer of the sterile saline wound...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2026· Medline Industries, LP

Recalled Item: Meijer STERILE saline wound wash Recalled by Medline Industries, LP Due to...

The Issue: Medline has identified that the manufacturer of the sterile saline wound...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) NAIL KIT Recalled by Medline Industries, LP Due...

The Issue: Medline has identified that the manufacturer of the sterile saline wound...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2026· Biomerieux Inc

Recalled Item: VITEK 2 Gram-negative Susceptibility Cards Containing o Polymyxin B (pb02n)...

The Issue: Potential risk of Quality Control failures and/or false resistant antibiotic...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2026· Encore Medical, LP

Recalled Item: EMPOWR 3D Knee Tibial Insert 5R 14MM Recalled by Encore Medical, LP Due to...

The Issue: 942-01-40G acetabular system package was found to contain 942-01-36H...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2026· Medline Industries, LP

Recalled Item: Medline Convenience Kits: 1) NAIL KIT Recalled by Medline Industries, LP Due...

The Issue: Medline has identified that the manufacturer of the sterile saline wound...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2026· Raz Design Inc

Recalled Item: Raz-AT (Attendant Tilt) Mobile Shower Commode Chair Recalled by Raz Design...

The Issue: Due to a modification by a vendor and may be reinstalled without properly...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 5, 2026· Encore Medical, LP

Recalled Item: EMPOWR Acetabular System: Liner Recalled by Encore Medical, LP Due to...

The Issue: 942-01-40G acetabular system package was found to contain 942-01-36H...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2026· Alphatec Spine, Inc.

Recalled Item: ATEC Lateral Navigation Disc Prep Instruments LIF NAV Recalled by Alphatec...

The Issue: Due a design issue where the navigated array connection geometry is incorrect.

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

Class II — Potential Health HazardOngoing