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. 2,723 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,723 in last 12 months

Showing 1872118740 of 30,921 recalls

Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom LOWER EXTREMITY convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Extension Line Adapters 20 in length Used to extend Recalled by...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom SHOULDER ARTHROSCOPY convenience kits Recalled by Avid...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom SPINE convenience kits Recalled by Avid Medical, Inc. Due to...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom MINOR PROCEDURE 6A convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· NeuroLogica Corporation

Recalled Item: The GC80 Digital X-ray Imaging System Recalled by NeuroLogica Corporation...

The Issue: An image was obtained with over exposure during a Thorax examination using...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom NEURO PK convenience kits Recalled by Avid Medical, Inc. Due...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom OBSTETRICAL PACK convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Cardioplegia Adapter with Pressure Port Provides access for a Recalled...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Medtronic Perfusion Systems

Recalled Item: DLP Pressure Monitoring Extension Line Adapters Extends the pressure line...

The Issue: Identification of small pinholes in a single packaging configuration of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom KNEE ARTHROSCOPY PACK convenience kits Recalled by Avid...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom DAVINCI PACK convenience kits Recalled by Avid Medical, Inc....

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 22, 2017· Avid Medical, Inc.

Recalled Item: AVID TruCustom HEART CATH TRAY convenience kits Recalled by Avid Medical,...

The Issue: Certain kits packed by the firm contain BD 22GA 1-1/2 inch SafetyGlide Non...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS MISS/MIS Compressor and Rod Tightener. Part of MAXIMIS...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 350 Straight Rod. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS MIS Screw5.5 x 55mm. Part of MAXIMIS Pedicle Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS Body Alignment Driver. Part of MAXIMIS Pedicle Screw...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 40mm Rod. Part of MAXIMIS Pedicle Screw Spinal Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS 60mm MIS Rod. Part of MAXIMIS Pedicle Screw Recalled by...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 21, 2017· Valorem Surgical LLC

Recalled Item: PALLAS M/MAXIMIS MIS Screw 6.5 x 40mm and 6.5 x Recalled by Valorem Surgical...

The Issue: Devices are not consistent with Quality System Requirements.

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

Class II — Potential Health HazardOngoing