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. 2,680 recalls have been distributed to Texas in the last 12 months.

55,713 total recalls
2,680 in last 12 months

Showing 2562125640 of 30,921 recalls

Medical DeviceSeptember 24, 2014· Joerns Healthcare

Recalled Item: Joerns EasyCare Bed Product Usage: The AC-powered adjustable hospital bed...

The Issue: The Easy-Care Care-Lock feature installed at the foot of the bed may...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zeego systems Recalled by Siemens Medical Solutions USA, Inc Due to A...

The Issue: A cable inside the C-arm systems may have been routed in an inappropriate...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 23, 2014· Invacare Corporation

Recalled Item: Invacare Perfecto 2 V Oxygen Concentrator The finished device is Recalled by...

The Issue: It was determined that a defective sieve bed subassembly enabled zeolite...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 22, 2014· Virtual Imaging, Inc.

Recalled Item: Digital Mobile X-ray Systems used to take diagnostic radiographic exposures...

The Issue: There is a potential for unintended and erratic motion.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· Siemens Healthcare Diagnostics

Recalled Item: IMMULITE /IMMULITE 1000 Systems COR Cortisol Recalled by Siemens Healthcare...

The Issue: Customer complaints were received for positive bias reported on the controls...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· GE Healthcare, LLC

Recalled Item: GE Healthcare Carescape Patient Data Module Recalled by GE Healthcare, LLC...

The Issue: GE Healthcare has recently become aware of a potential safety issue to the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: External power supply adaptors that accompany Clinitek Status+ The Clinitek...

The Issue: The external power supply for the Clintek Status analyzer, which is provided...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: External power supply adaptors that accompany Clinitek Status Power Supply...

The Issue: The external power supply for the Clintek Status analyzer, which is provided...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· Orthohelix Surgical Designs Inc

Recalled Item: MaxLock Extreme Mod-Foot Concave Reamer Recalled by Orthohelix Surgical...

The Issue: Incorrect sizing was being laser etched on the MaxLock Extreme Mod-Foot...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 19, 2014· Siemens Healthcare Diagnostics, Inc

Recalled Item: External power supply adaptors that accompany Clinitek Status Connect System...

The Issue: The external power supply for the Clintek Status analyzer, which is provided...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Covidien Kendall Adult Multi-Function Defibrillation Electrodes Part Number:...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: MediChoice¿ Multifunction Electrode Part Number: MC171 OH Recalled by...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Covidien Medi-Trace Cadence and Kendall Adult Multi-Function Defibrillation...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Philips HEARTSTART Multifunction Electrode Pads Part Number: M3718A Recalled...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Dokitz NovoSci

Recalled Item: Cardiopulmonary bypass connector Recalled by Dokitz NovoSci Due to The...

The Issue: The single leg of the PAY connector has been observed to become detached.

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2014· Intuitive Surgical, Inc.

Recalled Item: EndoWrist Stapler 45 instrument for the da Vinci Si System Recalled by...

The Issue: Intuitive is issuing an urgent product notice to all users of the EndoWrist...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Covidien Kendall 1710H Multi-Function Defibrillation Electrodes Part Number:...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 18, 2014· Covidien LLC

Recalled Item: Coviden Medi-Trace Cadence Adult Multi-Function Defibrillation Electrodes...

The Issue: Covidien Medi-Trace Cadence and Kendall Defibrillation Electrodes Not...

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

Class I — Serious Health HazardOngoing
Medical DeviceSeptember 17, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Artis zee/ zeego systems Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: The Small Focus of a 3 focal spot x-ray tube may fail and further release of...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 17, 2014· Cooper Vision Caribbean Corp.

Recalled Item: ProClear Toric contact lenses are made from a material containing Recalled...

The Issue: Routine quality monitoring system has identified that a limited number of...

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

Class III — Low RiskOngoing