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. 2,589 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,589 in last 12 months

Showing 36613680 of 13,432 recalls

DrugOctober 25, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Tadalafil Tablets Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Incorrect Product Formulation: An incorrect grade of Crospovidone was used...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 22, 2021· SUN PHARMACEUTICAL INDUSTRIES INC

Recalled Item: Pregabalin Capsules Recalled by SUN PHARMACEUTICAL INDUSTRIES INC Due to...

The Issue: Failed Tablet/Capsule Specifications: Out of Specification results for...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 20, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Gatifloxacin Ophthalmic Solution Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: Failed Stability Specifications: Out-of-specification results observed in a...

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

Class III — Low RiskOngoing
Refund
DrugOctober 19, 2021· Teligent Pharma, Inc.

Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by Teligent Pharma, Inc. Due...

The Issue: Defective Container

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2021· MERCK SHARP & DOHME CORP

Recalled Item: Cubicin (daptomycin for injection) Recalled by MERCK SHARP & DOHME CORP Due...

The Issue: Presence of Particulate Matter: Identified as Glass Particles

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 19, 2021· Teligent Pharma, Inc.

Recalled Item: Diclofenac Sodium Topical Solution USP Recalled by Teligent Pharma, Inc. Due...

The Issue: Defective Container

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 18, 2021· MACLEODS PHARMA USA, INC

Recalled Item: Rizatriptan Benzoate Film Coated Tablets Recalled by MACLEODS PHARMA USA,...

The Issue: Out-of-specification test results obtained in Organic Impurities test during...

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

Class III — Low RiskOngoing
Refund
DrugOctober 18, 2021· MACLEODS PHARMA USA, INC

Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets 5mg Recalled by MACLEODS...

The Issue: Out-of-specification test results obtained in Organic Impurities test during...

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

Class III — Low RiskOngoing
Refund
DrugOctober 18, 2021· MACLEODS PHARMA USA, INC

Recalled Item: Rizatriptan Benzoate Orally Disintegrating Tablets 10mg Recalled by MACLEODS...

The Issue: Out-of-specification test results obtained in Organic Impurities test during...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: Vica-Cet BACK PAIN RELIEF (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: PainAway II (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65 mg) tablets...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: ZEE+ painaid ESF Extra-Strength Formula (Acetaminophen 250 mg Recalled by...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: Afassco Pain Free Plus X-STRENGTH PAIN RELIEVER (Acetaminophen 250...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: Xpect First aid Extra Strength PAIN AWAY (Acetaminophen 250 mg/Aspirin...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: North by Honeywell PAIN STOPPER EXTRA STRENGTH (Acetaminophen 250 mg...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: AERO Tab PAIN RELIEVER (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine 65...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 13, 2021· Ultra Seal Corporation

Recalled Item: Advance Formula Pain Reliever (Acetaminophen 250 mg/Aspirin 250 mg/Caffeine...

The Issue: Failed Stability Specifications: Out-of-Specification results observed for...

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

Class III — Low RiskOngoing
Refund
DrugOctober 12, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 12, 2021· Teligent Pharma, Inc.

Recalled Item: Lidocaine Hydrochloride Topical Solution USP 4% (40 mg/mL) Recalled by...

The Issue: Superpotent Drug

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 12, 2021· Lupin Pharmaceuticals Inc.

Recalled Item: Irbesartan Tablets USP Recalled by Lupin Pharmaceuticals Inc. Due to CGMP...

The Issue: CGMP Deviations: impurity N-nitrosoirbesartan detected in API

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

Class II — Potential Health HazardOngoing
Refund