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. 2,606 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,606 in last 12 months

Showing 481500 of 48,595 recalls

Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

The Issue: Philips has identified that in a limited number of impacted systems the drip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

The Issue: Philips has identified that in a limited number of impacted systems the drip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· ICU Medical, Inc.

Recalled Item: Plum Duo Infusion System Recalled by ICU Medical, Inc. Due to ICU Medical...

The Issue: ICU Medical received one lot of defective primary speakers from our supplier...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

The Issue: Philips has identified that in a limited number of impacted systems the drip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

The Issue: Philips has identified that in a limited number of impacted systems the drip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10 Recalled by PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Due to...

The Issue: Philips has identified that in a limited number of impacted systems the drip...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

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

The Issue: Philips has identified that in a limited number of impacted systems the drip...

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

Class II — Potential Health HazardOngoing
FoodDecember 13, 2025· Tom Bumble LLC

Recalled Item: Tom Bumble Nutty Peanut Butter Flake Candy with Peanut & Recalled by Tom...

The Issue: Foreign material.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2025· Medinatura New Mexico, inc.

Recalled Item: ClearLife Allergy Nasal Spray Recalled by Medinatura New Mexico, inc. Due to...

The Issue: Microbial Contamination of Non-Sterile Products: The products have been...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 12, 2025· Medinatura New Mexico, inc.

Recalled Item: ReBoost Nasal Spray Recalled by Medinatura New Mexico, inc. Due to Microbial...

The Issue: Microbial Contamination of Non-Sterile Products: The products have been...

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 12, 2025· Merck Sharp & Dohme LLC

Recalled Item: Merck Emend (aprepitant) for oral suspension Recalled by Merck Sharp & Dohme...

The Issue: Presence of particulate matter: potential presence of metal particulates in...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 12, 2025· Merck Sharp & Dohme LLC

Recalled Item: Noxafil Powdermix (posaconazole) for Delayed-Release Oral Suspension...

The Issue: Presence of particulate matter: potential presence of metal particulates in...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 12, 2025· Bard Peripheral Vascular Inc

Recalled Item: Broviac 4.2 Fr Single-Lumen CV Catheter Cutdown Tray with SureCuff Recalled...

The Issue: Due to damage to outer tray that can potentially compromise the sterile barrier

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Elekta, Inc.

Recalled Item: Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment...

The Issue: Due to an error when defining a new stereotactic that users fail to first...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Elekta, Inc.

Recalled Item: Brand Name: Leksell GammaPlan Product Name: Radionuclide RT Treatment...

The Issue: Due to an error when defining a new stereotactic that users fail to first...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) WATKINS SPINE...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) BREAST-HERNIA-PORT...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: 1) SMJ LAP Recalled...

The Issue: Medline kits were manufactured and distributed containing MASTISOL liquid...

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

Class II — Potential Health HazardOngoing