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. 1,872 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,872 in last 12 months

Showing 1748117500 of 48,595 recalls

DrugJuly 11, 2020· 4e Brands North America, Llc

Recalled Item: ASSURED Instant Hand Sanitizer Aloe & Moisturizers Recalled by 4e Brands...

The Issue: CGMP Deviations: recalled because it was manufactured in the same facility...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2020· 4e Brands North America, Llc

Recalled Item: blumen ADVANCED HAND SANITIZER Recalled by 4e Brands North America, Llc Due...

The Issue: CGMP Deviations: recalled because it was manufactured in the same facility...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2020· 4e Brands North America, Llc

Recalled Item: blumen Clear ADVANCED HAND SANITIZER with 70% ALCOHOL Recalled by 4e Brands...

The Issue: Chemical Contamination and Subpotent Drug: Product tested to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 11, 2020· 4e Brands North America, Llc

Recalled Item: blumen ADVANCED INSTANT HAND SANITIZER Clear ETHYL ALCOHOL 70% natural...

The Issue: Chemical Contamination and Subpotent Drug: Product tested to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 11, 2020· 4e Brands North America, Llc

Recalled Item: blumen Aloe ADVANCED HAND SANITIZER 70% ALCOHOL CONTENT (70% ethyl alcohol...

The Issue: CGMP Deviations: recalled because it was manufactured in the same facility...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2020· 4e Brands North America, Llc

Recalled Item: blumen ADVANCED INSTANT HAND SANITIZER Clear ETHYL ALCOHOL 70% Natural...

The Issue: CGMP Deviations: recalled because it was manufactured in the same facility...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 11, 2020· 4e Brands North America, Llc

Recalled Item: blumen ADVANCED HAND SANITIZER 70% ALCOHOL CONTENT Recalled by 4e Brands...

The Issue: Chemical Contamination and Subpotent Drug: Product tested to contain...

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 10, 2020· Keryx Biopharmaceuticals, Inc.

Recalled Item: Auryxia (ferric citrate) tablets 210 mg Recalled by Keryx...

The Issue: cGMP deviations: Lots recalled were not manufactured in conformance with the...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 9, 2020· Maquiladora Miniara Sa De Cv

Recalled Item: Shine & Clean Hand Sanitizer gel Recalled by Maquiladora Miniara Sa De Cv...

The Issue: CGMP Deviations: Products manufactured at the same site were FDA testing...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 9, 2020· Medline Industries Inc

Recalled Item: Endoscopic Cleaning Brush - Product Usage: Endoscopic cleaning brushes are...

The Issue: Potential risk of brush detachment during cleaning.

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· New Wave Endo-Surgical, Corp.

Recalled Item: M-Close Kit Recalled by New Wave Endo-Surgical, Corp. Due to The plastic...

The Issue: The plastic housing on the device may fracture

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 8, 2020· Flower Orthopedics Corporation

Recalled Item: Calcaneus Plate Recalled by Flower Orthopedics Corporation Due to The...

The Issue: The contract manufacturer of the calcaneus plate inadvertently used the...

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

Class II — Potential Health HazardOngoing
DrugJuly 7, 2020· Mylan Institutional LLC

Recalled Item: Daptomycin for Injection Recalled by Mylan Institutional LLC Due to Presence...

The Issue: Presence of Particulate Matter

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

Class I — Serious Health HazardOngoing
Refund
DrugJuly 6, 2020· Allergan PLC

Recalled Item: Skin Medica Acne System Recalled by Allergan PLC Due to SUBPOTENT DRUG:...

The Issue: SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.

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

Class III — Low RiskOngoing
Refund
DrugJuly 6, 2020· Allergan PLC

Recalled Item: Skin Medica Acne Treatment Lotion (Benzoyl Peroxide 2.5%) Recalled by...

The Issue: SUBPOTENT DRUG: Products failed assay results at the 12 and 24 month timepoints.

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

Class III — Low RiskOngoing
Refund