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. 2,343 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,343 in last 12 months

Showing 481500 of 48,595 recalls

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 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· SunMed Holdings, LLC

Recalled Item: Brand Name: Broselow Product Name: Broselow Domestic Complete ALS Organizer...

The Issue: Product contains potentially harmful dosing errors for Vecuronium,...

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

Class I — Serious 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
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Product Name: Allura Xper FD10C Recalled by PHILIPS MEDICAL SYSTEMS...

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 15, 2025· WhiteWave - Louisville Pilot Plant

Recalled Item: So Delicious Dairy Free Salted Caramel Cluster Cashewmilk Recalled by...

The Issue: Foreign material

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 15, 2025· NOVADOZ PHARMACEUTICALS LLC

Recalled Item: Glycopyrrolate Oral Solution Recalled by NOVADOZ PHARMACEUTICALS LLC Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 15, 2025· PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.

Recalled Item: Allura Xper FD10/10 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
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
Medical DeviceDecember 12, 2025· Medline Industries, LP

Recalled Item: Medline medical procedure convenience kits labeled as: CIRCUMCISION PACK...

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) INPATIENT CTRL...

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· NIPRO Technical Services, Inc.

Recalled Item: Conductivity Standard Solution Catalog/Model Numbers: 10001 Recalled by...

The Issue: due to a defect associated with the conductivity values of the solution used...

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) MEM MAXILLOFACIAL...

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· 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) MIDDLE EAR CDS...

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· 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
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
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
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