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 341360 of 30,921 recalls

Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) PACER / Recalled...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) MEM MAXILLOFACIAL...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) MIDDLE EAR CDS...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· NIPRO Technical Services, Inc.

Recalled Item: Conductivity Standard Solution Catalog/Model Numbers: 10001 Recalled by...

The Issue: due to a defect associated with the conductivity values of the solution used...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Hologic, Inc

Recalled Item: ThinPrep¿ CytoLyt¿ Solution. Buffered Cell Wash Solution. Recalled by...

The Issue: Fungal contamination of affected lot with Parengyodontium album.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Philips Azurion Systems with software versions R2.1.10 and R2.2.10. Includes...

The Issue: Six (6) identified software issues which may result in the following: system...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Codman Microsensor Basic Kit. Catalog Number: 626631US. Use of the Recalled...

The Issue: Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Philips North America Llc

Recalled Item: Philips Smart-hopping 2.0 AP 1.4 GHz. Patient Monitor. Recalled by Philips...

The Issue: It was found that the MX40 device could not reconnect to the PIC iX when...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Integra LifeSciences Corp. (NeuroSciences)

Recalled Item: Codman CereLink ICP Sensor Basic Kit. Catalog Number: 826850. The Recalled...

The Issue: Potential corrosion stains on the surface of the 14-gauge Tuohy Needle that...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2025· Fujirebio Diagnostics, Inc.

Recalled Item: Product Name: Lumipulse pTau 217 Plasma Controls Model/Catalog Number: 81558...

The Issue: Customers may experience inaccurate test results by observing a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2025· Fujirebio Diagnostics, Inc.

Recalled Item: Product Name: Lumipulse G pTau 217 Plasma Calibrators Model/Catalog Number:...

The Issue: Customers may experience inaccurate test results by observing a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2025· Fujirebio Diagnostics, Inc.

Recalled Item: Product Name: Lumipulse G pTau217/B-Amyloid 1-42 Plasma Ratio Model/Catalog...

The Issue: Customers may experience inaccurate test results by observing a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2025· Fujirebio Diagnostics, Inc.

Recalled Item: Product Name: Lumipulse ¿-Amyloid Plasma Controls Model/Catalog Number:...

The Issue: Customers may experience inaccurate test results by observing a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2025· Fujirebio Diagnostics, Inc.

Recalled Item: Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Immunoreaction Cartridges...

The Issue: Customers may experience inaccurate test results by observing a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2025· Fujirebio Diagnostics, Inc.

Recalled Item: Product Name: Lumipulse G ¿-Amyloid 1-42-N Plasma Calibrators Model/Catalog...

The Issue: Customers may experience inaccurate test results by observing a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2025· Fujirebio Diagnostics, Inc.

Recalled Item: Product Name: Lumipulse G pTau 217 Plasma Immunoreaction Cartridges...

The Issue: Customers may experience inaccurate test results by observing a higher...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 11, 2025· Instrumentation Laboratory

Recalled Item: The product is used for the evaluation of the intrinsic coagulation pathway...

The Issue: Potential for microbial contamination.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2025· Mazor Robotics Ltd

Recalled Item: Mazor X robotic guidance system Recalled by Mazor Robotics Ltd Due to...

The Issue: Software errors that can result in incorrect surgical instrument positioning...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 10, 2025· Elekta, Inc.

Recalled Item: MOSAIQ Oncology Information System with Particle Therapy License (License...

The Issue: Using oncology information system that manages workflow may result in...

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

Class II — Potential Health HazardOngoing