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 1758117600 of 30,921 recalls

Medical DeviceFebruary 12, 2018· Arjohuntleigh Magog

Recalled Item: Q-Connect 272 KG Scale used with Maxi Sky 2 ceiling Recalled by...

The Issue: The spreader bar can detach from the scale attachment under certain conditions.

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT(R) ClearVUE(R) isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Stanbio Laboratory, LP

Recalled Item: Stanbio AC power adapter for the HemoPoint H2 meter Recalled by Stanbio...

The Issue: The US prong (type A) adapter plate may crack, break, or detach and remain...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore (Radiology) - Model no. 728244 Recalled by Philips...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE isp Implantable Port With Smooth Septum and Attachable...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Tornier, Inc

Recalled Item: Fornier Phantom Fiber(TM) Sutures: Item Number Description SMB000425 4.5 MM...

The Issue: Data has shown that degradation of a raw material used in Phantom Fiber may...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Life Technologies Corporation

Recalled Item: Oncomine Dx Target Test Recalled by Life Technologies Corporation Due to The...

The Issue: The lower concentration of the RNA panel could cause a NO CALL or FALSE...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Bard Peripheral Vascular Inc

Recalled Item: POWERPORT ClearVUE Slim with Smooth Septum Recalled by Bard Peripheral...

The Issue: The Patient ID Card packaged with the POWERPORT ClearVUE Implantable Port...

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

Class II — Potential Health HazardOngoing
Medical DeviceFebruary 8, 2018· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 - Model no. 728231 Recalled by Philips Medical Systems...

The Issue: Closing the Emergency Stop may disable the horizontal motor, allowing the...

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

Class II — Potential Health HazardOngoing