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. 2,572 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,572 in last 12 months

Showing 68016820 of 48,595 recalls

Medical DeviceDecember 27, 2023· Abiomed, Inc.

Recalled Item: Impella catheters - Intravascular micro axial blood pumps that support...

The Issue: IFU has been updated to include warnings about the risk of the inlet...

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

Class I — Serious Health HazardOngoing
DrugDecember 26, 2023· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Divalproex Sodium Extended-release Tablets Recalled by Amneal...

The Issue: Failed dissolution specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 26, 2023· Haleon US Holdings LLC

Recalled Item: Robitussin Honey CF Max Nighttime Adult (Acetaminophen 650 mg Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 26, 2023· Haleon US Holdings LLC

Recalled Item: Robitussin Honey CF Max Non-Drowsy Adult (Acetaminophen 650mg Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 26, 2023· Amerisource Health Services LLC

Recalled Item: Benzonatate Capsules Recalled by Amerisource Health Services LLC Due to...

The Issue: Superpotent drug: Assay results were slightly above specification at the...

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

Class III — Low RiskOngoing
Refund
Medical DeviceDecember 26, 2023· GE Medical Systems, SCS

Recalled Item: Senographe Pristina Recalled by GE Medical Systems, SCS Due to X-ray...

The Issue: X-ray exposure termination audible signal on Senographe Pristina with...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2023· Ossur H / F

Recalled Item: Power Knee Recalled by Ossur H / F Due to Knee batteries may need...

The Issue: Knee batteries may need replacement with conforming batteries to ensure...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Onkos Surgical, Inc.

Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling

The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Onkos Surgical, Inc.

Recalled Item: ELEOS COLLAR STEM Recalled by Onkos Surgical, Inc. Due to Mislabeling

The Issue: Mislabeling of 13mm Modular Segmental Stem package (HC-13120-03M) which...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Howmedica Osteonics Corp.

Recalled Item: HRIS ACET CUP CUT TIP 26X140 Part Number: 6210-5-100. single-use Recalled by...

The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 22, 2023· Howmedica Osteonics Corp.

Recalled Item: HRIS ACET CUP CUT TIP 32X140 Part Number: 6210-5-200rker. single-use...

The Issue: Failed to meet the acceptance criteria for the seal integrity and/or package...

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

Class II — Potential Health HazardOngoing
FoodDecember 21, 2023· County Fair Foods, Inc.

Recalled Item: Popcorn Pre-Pop in 8oz Polypropylene bag packaged 20 bags to a case Recalled...

The Issue: Undeclared Yellow #5

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Insight Pharmaceuticals LLC, a Prestige Consumer Healthcare company

Recalled Item: Americaine Recalled by Insight Pharmaceuticals LLC, a Prestige Consumer...

The Issue: Chemical Contamination: presence of benzene

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2023· PFIZER

Recalled Item: Bleomycin for Injection Recalled by PFIZER Due to Presence of particulate...

The Issue: Presence of particulate matter: glass

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: Freskaro & revitalize Magnesium Citrate Saline Laxative Oral Solution...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: Good Neighbor Pharmacy Recalled by Pharma Nobis LLC Due to MICROBIAL...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Pfizer Inc.

Recalled Item: 4.2% Sodium Bicarbonate Injection Recalled by Pfizer Inc. Due to Presence of...

The Issue: Presence of Particulate Matter; identified as glass

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

Class I — Serious Health HazardOngoing
Refund
DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: CVS Health Magnesium Citrate Saline Laxative Oral Solution DYE FREE Recalled...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Pharma Nobis LLC

Recalled Item: Freskaro & revitalize Magnesium Citrate Saline Laxative Oral Solution...

The Issue: MICROBIAL CONTAMINATION OF NON-STERILE PRODUCTS - Presence of Acetobacter...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 21, 2023· Pfizer Inc.

Recalled Item: 8.4 % Sodium Bicarbonate Injection Recalled by Pfizer Inc. Due to Presence...

The Issue: Presence of Particulate Matter; identified as glass

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

Class I — Serious Health HazardOngoing
Refund