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. 1,116 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,116 in last 12 months

Showing 2281–2300 of 27,850 recalls

Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Cardio Vascular-Allura Centron Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10C Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 - Catalog numbers: (1) 722003 Recalled by PHILIPS MEDICAL...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 OR Table Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Biplane Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V....

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 3 M15 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 5 M12 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura CV20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20/15 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 7 M20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Azurion 3 M12 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 13, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD20 Biplane OR Table Recalled by PHILIPS MEDICAL SYSTEMS...

The Issue: Possibility of the patient falling from the table related to the mattress...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2025· Nobel Biocare

Recalled Item: . Nobel Biocare N1 TiUltra TCC RP 4.0x9mm . Nobel Recalled by Nobel Biocare...

The Issue: Due to manufacturing issue (unintended by-product of the injection molding...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2025· Spectranetics Corporation

Recalled Item: Intact Vascular Tack Endovascular System Recalled by Spectranetics...

The Issue: Use of Tack Endovascular system, designed to treat acute dissections of...

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

Class I — Serious Health HazardOngoing
Medical DeviceJanuary 10, 2025· Integra LifeSciences Corp.

Recalled Item: Brand Name: MediHoney¿ Gel Product Name: MediHoney¿ Wound & Burn Recalled by...

The Issue: Potential that the induction seal is not completely sealed to the device...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 10, 2025· CareFusion 303, Inc.

Recalled Item: BD Pyxis: MedFlex Recalled by CareFusion 303, Inc. Due to Automated...

The Issue: Automated dispensing device labeling is being updated to strengthen labeling...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 9, 2025· Medtronic Neuromodulation

Recalled Item: A820 myPTM Software Application associated with Medtronic SynchroMed Pump...

The Issue: Product complaints were received describing the A820 myPTM app taking longer...

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

Class II — Potential Health HazardOngoing