Product Recalls in New Mexico

Product recalls affecting New Mexico — including food, drugs, consumer products, medical devices, and vehicles distributed to New Mexico. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,026 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,026 in last 12 months

Showing 16681–16700 of 48,595 recalls

Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number U1053617 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053616 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Luminex Corporation

Recalled Item: Verigene Gram Negative Blood Culture Nucleic Acid Test (BC-GN) Model...

The Issue: Potential for a false-negative result.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Luminex Corporation

Recalled Item: Verigene Respiratory Pathogens Flex Nucleic Acid Test (RP Flex) Model...

The Issue: Potential for a false-negative result.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1076709 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1076717 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number DU1053617 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Luminex Corporation

Recalled Item: Verigene Clostridium difficile Nucleic Acid Test Kit (CDF) Model Number:...

The Issue: Potential for a false-negative result.

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Plus Ventilator Part Number 1137276 - Product...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053618 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053617 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053614 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053613 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1076716 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 30, 2020· Respironics California, LLC

Recalled Item: Philips Respironics V60 Ventilator Part Number 1053615 - Product Usage:...

The Issue: Ventilator may experience potential issues with the backup battery failures:...

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

Class II — Potential Health HazardOngoing
DrugOctober 30, 2020· AVKARE Inc.

Recalled Item: Mesalamine Delayed-Release Tablets Recalled by AVKARE Inc. Due to Failed...

The Issue: Failed Dissolution Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 29, 2020· Prytime Medical Devices, Inc.

Recalled Item: PryTime Medical - ER-Reboa Plus Catheter Recalled by Prytime Medical...

The Issue: There is a potential that catheters may have incorrectly marked balloon and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2020· Chromsystems Instruments & Chemicals GmbH

Recalled Item: MassChrom Cortisol Recalled by Chromsystems Instruments & Chemicals GmbH Due...

The Issue: Control lots may not meet stability criteria and could result in increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2020· Chromsystems Instruments & Chemicals GmbH

Recalled Item: MassChrom Cortisol Recalled by Chromsystems Instruments & Chemicals GmbH Due...

The Issue: Control lots may not meet stability criteria and could result in increased...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2020· Chromsystems Instruments & Chemicals GmbH

Recalled Item: 6PLUS1 Multilevel Saliva Calibrator Set Cortisol Cortisone in Saliva...

The Issue: Calibrator lots may not meet stability criteria and could result in...

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

Class II — Potential Health HazardOngoing