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. 2,600 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,600 in last 12 months

Showing 281300 of 30,921 recalls

Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Volk Single Use Vitrectomy Lenses 1. Flat Vitrectomy Lens Recalled by Vortex...

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· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) THORACIC ROBOTICS...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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 Lindsell Sutured IOL Marker Recalled by Vortex Surgical Inc....

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· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: KIT ROBOTICS UROLOGY...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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: Oertli 1. 23G Laser Probe OS4 Flex-Tip VK401113 2. 23G Recalled by Vortex...

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: 25GA Subretinal Injection Cannula VS0220.25 Recalled by Vortex Surgical Inc....

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 25GA I.D.D. Internal Delivery Device Recalled by Vortex...

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: Rumex Disposable Diamond Dusted ILM Elevator Recalled by Vortex Surgical...

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 Disposable Forceps and Cannula 1. 23GA ACTU8 Forceps Adaptive...

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 25GA Backflush Recalled by Vortex Surgical Inc. Due to There...

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· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAVH PROCEDURE...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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 TID Pharos Illuminated Depressor Recalled by Vortex Surgical...

The Issue: XXX

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
Medical DeviceDecember 16, 2025· Vortex Surgical Inc.

Recalled Item: Tecfen Retractable Membrane Polisher 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
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· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) LAPAROSCOPY CDS-LF...

The Issue: Medline kits containing Stryker's Strykeflow 2 Suction Irrigators due to a...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2025· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

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

Class I — Serious Health HazardOngoing
Medical DeviceDecember 15, 2025· Hologic, Inc

Recalled Item: Brevera Breast Biopsy System Disposable 9 Gauge Needle. Biopsy Instrument....

The Issue: Presence of particulates in affected devices that can be deposited into...

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

Class II — Potential Health HazardOngoing