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 1001–1020 of 48,595 recalls

Medical DeviceOctober 14, 2025· Beckman Coulter Ireland, Inc.

Recalled Item: BECKMAN COULTER BICARBONATE OSR6237 OSR6637 OSR6x37 Bicarbonate is Recalled...

The Issue: Bicarbonate reagent may generate falsely high Bicarbonate results due to...

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

Class II — Potential Health HazardOngoing
DrugOctober 14, 2025· FARMAKEIO OUTSOURCING LLC

Recalled Item: Testosterone Regular Release 50 MG Recalled by FARMAKEIO OUTSOURCING LLC Due...

The Issue: CGMP Deviations: Potential presence of metal particulate matter

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 14, 2025· FARMAKEIO OUTSOURCING LLC

Recalled Item: Testosterone / Triamcinolone Acetonide Pellet (200MG/40MCG) Recalled by...

The Issue: CGMP Deviations: Potential presence of metal particulate matter

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 14, 2025· FARMAKEIO OUTSOURCING LLC

Recalled Item: Testosterone / Triamcinolone Acetonide 87.5MG/17.5MCG Recalled by FARMAKEIO...

The Issue: CGMP Deviations: Potential presence of metal particulate matter

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 13, 2025· Paragon 28, Inc.

Recalled Item: Phantom Fibula Nail Recalled by Paragon 28, Inc. Due to Fibula nail system...

The Issue: Fibula nail system intended for use in fixation of fibular fractures and...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 13, 2025· MRIMed Inc.

Recalled Item: MRI LED Mobile Exam Light Battery This non-magnetic Recalled by MRIMed Inc....

The Issue: Due to battery component overheating while charging resulting in melting of...

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

Class II — Potential Health HazardOngoing
DrugOctober 10, 2025· Alembic Pharmaceuticals Limited

Recalled Item: Fesoterodine Fumarate Recalled by Alembic Pharmaceuticals Limited Due to...

The Issue: Failed Impurities/Degradation Specifications: Due to levels of 'Diester...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
DrugOctober 10, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 2.5 mg Recalled by Endo USA, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 10, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 7.5mg Recalled by Endo USA, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience Kits: DYNJ901048N ORTHO SPINE ST CLAIR DYNJ909123F UROLOGY MINOR...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
DrugOctober 10, 2025· QuVa Pharma, Inc.

Recalled Item: R.E.C.K. (Ropivacaine HCl Recalled by QuVa Pharma, Inc. Due to Presence of...

The Issue: Presence of Particulate Matter

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Convenience kits Recalled by Medline Industries, LP Due to Firm received...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
DrugOctober 10, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: an out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2025· Lannett Company Inc.

Recalled Item: Niacin Extended-release Tablets Recalled by Lannett Company Inc. Due to...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2025· The Harvard Drug Group LLC

Recalled Item: Gabapentin Capsules Recalled by The Harvard Drug Group LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: an out of specification result...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 10, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 5mg Recalled by Endo USA, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund
Medical DeviceOctober 10, 2025· Medline Industries, LP

Recalled Item: Anesthesia Circuit Kits and other various kits that contain Anesthesia...

The Issue: Firm received multiple complaints of anesthesia circuit leaks due to cracks...

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

Class I — Serious Health HazardOngoing
DrugOctober 10, 2025· Endo USA, Inc.

Recalled Item: Everolimus tablets 10 mg Recalled by Endo USA, Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of specification for...

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

Class III — Low RiskOngoing
Refund