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. 1,862 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,862 in last 12 months

Showing 2264122660 of 48,595 recalls

Medical DeviceJanuary 22, 2019· Ortho-Clinical Diagnostics

Recalled Item: VITROS Chemistry Products Na+ Slides Recalled by Ortho-Clinical Diagnostics...

The Issue: Imprecision in the affected lot may produce negatively or positively biased...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 19, 2019· GE Healthcare, LLC

Recalled Item: Revolution CT scanners Product Usage: The system is intended for head...

The Issue: Additional low dose radiation exposure.

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

Class II — Potential Health HazardOngoing
DrugJanuary 18, 2019· Mylan Institutional, Inc. (d.b.a. UDL Laboratories)

Recalled Item: Alprazolam Tablets Recalled by Mylan Institutional, Inc. (d.b.a. UDL...

The Issue: Failed Impurities/Degradation Specifications: Elevated levels of a known...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2019· Prinston Pharmaceutical Inc

Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2019· Mylan Pharmaceuticals Inc.

Recalled Item: Fexofenadine HCl Tablets Recalled by Mylan Pharmaceuticals Inc. Due to...

The Issue: Failed Impurities/Degradation Specifications: Related compound results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2019· Prinston Pharmaceutical Inc

Recalled Item: Irbesartan Tablets 300 mg 90 count Rx only Manufactured by: Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2019· Prinston Pharmaceutical Inc

Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2019· Prinston Pharmaceutical Inc

Recalled Item: Irbesartan and Hydrochlorothiazide Tablets Recalled by Prinston...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 18, 2019· Prinston Pharmaceutical Inc

Recalled Item: Irbesartan and HydrochlorothiazideTablets Recalled by Prinston...

The Issue: CGMP Deviations: FDA lab confirmed presence an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 18, 2019· Bellus Medical

Recalled Item: SKINFUSE Resuce Calming Complex Kit containing: SKINFUSE LIFT HG - Recalled...

The Issue: Cosmetic Kit was packaged with a mislabel medical product.

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 17, 2019· CryoLife, Inc.

Recalled Item: On-X Aortic Heart Valve with Anatomic Sewing Ring Product Usage: Recalled by...

The Issue: On-X Valve was mislabeled with the incorrect serial number.

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

Class II — Potential Health HazardOngoing
DrugJanuary 16, 2019· KRS Global Biotechnology, Inc

Recalled Item: NORepinephrine 16 mg added to 0.9% Sodium Chloride (PF) Recalled by KRS...

The Issue: Labeling: Label mix-up

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 16, 2019· KRS Global Biotechnology, Inc

Recalled Item: NORepinephrine 4 mg added to 5% Dextrose 250 mL Bag (PF) Recalled by KRS...

The Issue: Labeling: Label mix-up

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 16, 2019· Polymer Technology Systems, Inc.

Recalled Item: CHOL+HDL+GLU test strips Recalled by Polymer Technology Systems, Inc. Due to...

The Issue: Some lots of test strips do not fit tightly into the optical block, and may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2019· Polymer Technology Systems, Inc.

Recalled Item: Lipid Panel test strips (as a component of smart bundles) Recalled by...

The Issue: Some lots of test strips do not fit tightly into the optical block, and may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2019· Polymer Technology Systems, Inc.

Recalled Item: Lipid Panel test strips Recalled by Polymer Technology Systems, Inc. Due to...

The Issue: Some lots of test strips do not fit tightly into the optical block, and may...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 16, 2019· Edwards Lifesciences, LLC

Recalled Item: Edwards Lifesciences(R) IntraClude(TM) Intra-Aortic Occlusion Device is a...

The Issue: Edwards Lifesciences has received a limited number of customer reports...

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

Class II — Potential Health HazardOngoing
DrugJanuary 15, 2019· Tris Pharma Inc.

Recalled Item: infants* IBUPROFEN Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2019· Tris Pharma Inc.

Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 15, 2019· Tris Pharma Inc.

Recalled Item: Infants' Ibuprofen Recalled by Tris Pharma Inc. Due to Superpotent Drug:...

The Issue: Superpotent Drug: recalled lots may have higher concentration of ibuprofen...

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

Class II — Potential Health HazardOngoing
Refund