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. 1,006 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,006 in last 12 months

Showing 17601–17620 of 48,595 recalls

Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004550002 GTIN: 14026704663061 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· OrthoPediatrics Corp

Recalled Item: Orthopedics 6.0MM ROD Recalled by OrthoPediatrics Corp Due to Product may...

The Issue: Product may have incorrect laser etched alignment lines, the non-conforming...

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004551004 GTIN: 24026704553796 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 0004550003 GTIN: 14026704663078 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004551035 GTIN:7290102156443 (each) - Product...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004551003 GTIN: 14026704663122 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004551002 GTIN: 14026704663115 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· TELEFLEX MEDICAL INC

Recalled Item: Rusch Greenlite Product Code: 004550004 GTIN: 14026704663085 (each) -...

The Issue: Breaking at the point of a welded joint

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 6, 2020· Sysmex America, Inc.

Recalled Item: Sysmex PS-10 Sample Preparation System Catalog number:BQ716341 - Product...

The Issue: Insufficient amount of antibody without an error message or alarm

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

Class II — Potential Health HazardOngoing
Medical DeviceJuly 5, 2020· Dynex Technologies, Inc.

Recalled Item: DYNEX Agility Recalled by Dynex Technologies, Inc. Due to Control samples...

The Issue: Control samples aspirated from wrong SmartKit on the Agility. Agility...

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

Class II — Potential Health HazardOngoing
DrugJuly 3, 2020· Granules Pharmaceuticals Inc

Recalled Item: Metformin Hydrochloride Extended-Release Tablets USP Recalled by Granules...

The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Tadalafil 18 mg Capsule Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Minoxidil/Biotin 1.25mg/5mg Capsule Recalled by MasterPharm LLC Due to Lack...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Formula 82F (Minoxidil 5%/Tretinoin 0.01%/Fluocinolone Acetonide...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Sildenafil 50 mg Troche Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Progesterone 300 mg Troche Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Yohimbine HCL 5.4mg Capsule Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Calcium citrate tetrahydrate USP powder Recalled by MasterPharm LLC Due to...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: D-Biotin 300 mg Capsule Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 2, 2020· MasterPharm LLC

Recalled Item: Tadalafil 12 mg Capsule Recalled by MasterPharm LLC Due to Lack of...

The Issue: Lack of Processing Controls (lack of assurance of conformity to specifications).

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

Class II — Potential Health HazardOngoing
Refund