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. 2,579 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,579 in last 12 months

Showing 54215440 of 48,595 recalls

Medical DeviceMay 16, 2024· Medtronic Perfusion Systems

Recalled Item: TourniKwik Tourniquet Set (CFN 79012) Recalled by Medtronic Perfusion...

The Issue: Incorrect component placed in four manufactured lots of the TourniKwik"...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· BioFire Diagnostics, LLC

Recalled Item: BIOFIRE FILMARRAY Gastrointestinal (GI) Panel (30 test kit) Recalled by...

The Issue: Due to increase of false positive Vibrio/Vibrio Cholerae results when using...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim XR 5 Implantable Pulse Generator Recalled by Abbott Medical...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim 5 Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim 7 Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim XR 7 Implantable Pulse Generator Recalled by Abbott Medical...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim Plus 7 Implantable Pulse Generator Recalled by Abbott...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim Plus 5 Implantable Pulse Generator Recalled by Abbott...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim DRG Implantable Pulse Generator Recalled by Abbott Medical...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim Plus 5 Implantable Pulse Generator Recalled by Abbott...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim 5 Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Proclaim 7 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Proclaim 7 Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Proclaim 5 Elite Implantable Pulse Generator Recalled by Abbott Medical Due...

The Issue: The duration between the implantable pulse generator reaching the elective...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Abbott Medical

Recalled Item: Abbott Liberta RC Recalled by Abbott Medical Due to Deep brain stimulation...

The Issue: Deep brain stimulation system will first turn off after approximately 50...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 16, 2024· Inspire Medical Systems Inc.

Recalled Item: Inspire Model 3028 Recalled by Inspire Medical Systems Inc. Due to There is...

The Issue: There is a potential manufacturing defect which can lead to electrical...

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

Class I — Serious Health HazardOngoing
Medical DeviceMay 16, 2024· Fresenius Medical Care Holdings, Inc.

Recalled Item: US AquaA 900H-Typ USA-3 x 208v-Intended for the purification of Recalled by...

The Issue: Concentrate Flow was exceeding the maximum 19.9 bar set point. The standard...

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

Class II — Potential Health HazardOngoing
DrugMay 15, 2024· Regeneron Pharmaceuticals Inc

Recalled Item: EYLEA Recalled by Regeneron Pharmaceuticals Inc Due to Lack of Assurance of...

The Issue: Lack of Assurance of Sterility: Complaints of syringe breakage

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 15, 2024· Medtronic Neuromodulation

Recalled Item: A610 Clinician Programmer (CP) Software Application (app) with the following...

The Issue: Patients implanted with a pocket adaptor (Model 64001 and/or 64002) are...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 15, 2024· American Contract Systems Inc

Recalled Item: UPPER EXTREMITY PK Recalled by American Contract Systems Inc Due to Ethylene...

The Issue: Ethylene Oxide/Ethylene Chlorohydrin (EO/ECH) residuals for the cast padding...

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

Class II — Potential Health HazardOngoing