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. 1,078 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
1,078 in last 12 months

Showing 9541–9560 of 48,595 recalls

DrugMarch 17, 2023· Ascend Laboratories, LLC

Recalled Item: Aripiprazole Tablets Recalled by Ascend Laboratories, LLC Due to Out of...

The Issue: Out of specification (OOS) for Spectroscopic Identification test by IR.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 17, 2023· Amerisource Health Services LLC

Recalled Item: Glimepiride Tablets Recalled by Amerisource Health Services LLC Due to CGMP...

The Issue: CGMP Deviations: recalling drug products following an FDA inspection.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 17, 2023· Steris Corporation

Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...

The Issue: Light handle covers may separate from the light handle (detach and fall off)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Philips North America Llc

Recalled Item: Spectral CT 7500 Computed Tomography X-Ray System Recalled by Philips North...

The Issue: Pressing the Unload Pedal of the foot switch to perform the unload function...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Medtronic Neuromodulation

Recalled Item: Medtronic SenSight Extension Tunneler Kit Recalled by Medtronic...

The Issue: Medtronic has received reports of SenSight Extension Tunneler kits that...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Steris Corporation

Recalled Item: Steris Lighting and Visualization Systems Recalled by Steris Corporation Due...

The Issue: Light handle covers may separate from the light handle (detach and fall off)...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2023· Beaver Visitec International, Inc.

Recalled Item: CryoTreQ- Aa disposable handheld instrument intended for ophthalmic surgery....

The Issue: Device suddenly and forcefully disassembled after cryotherapy, potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Centaur Cortisol 50T (Material Number 10994924) Recalled by Siemens...

The Issue: There is a negative bias with urine patient samples and urine cortisol...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2023· Ellex Medical Pty Ltd.

Recalled Item: Integre Pro Yellow LP561 Recalled by Ellex Medical Pty Ltd. Due to When...

The Issue: When using a Laser-Indirect-Ophthalmoscope (LIO) as the delivery device, a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2023· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Atellica IM Cortisol 50T (Material Number 10995538) Recalled by Siemens...

The Issue: There is a negative bias with urine patient samples and urine cortisol...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2023· SPINEART SA

Recalled Item: JULIET Ti LL Recalled by SPINEART SA Due to JULIET Lateral Lumbar Ti-Life...

The Issue: JULIET Lateral Lumbar Ti-Life Plate, a component of the JULIET Ti Lateral...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 16, 2023· Carefusion 2200 Inc

Recalled Item: (1) Carefusion V. Mueller Graves Vaginal Speculum Recalled by Carefusion...

The Issue: A portion of the two products were incorrectly marked (etched) and packaged...

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

Class II — Potential Health HazardOngoing
DrugMarch 16, 2023· Northwind Pharmaceuticals LLC

Recalled Item: Doxazosin Tablets Recalled by Northwind Pharmaceuticals LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 16, 2023· Scenic Fruit Company, LLC

Recalled Item: Trader Joes Organic Tropical Fruit Blend Recalled by Scenic Fruit Company,...

The Issue: Potential to be contaminated with hepatitis A.

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 16, 2023· Focus Health Group Inc

Recalled Item: Epinephrine Professional EMS Recalled by Focus Health Group Inc Due to...

The Issue: Labeling; Incorrect NDC number on outer carton of product.

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

Class III — Low RiskOngoing
Refund
DrugMarch 16, 2023· Amerisource Health Services LLC

Recalled Item: Verapamil Hydrochloride Extended-Release Tablets Recalled by Amerisource...

The Issue: Failed Dissolution Specifications: Out of specification dissolution results...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2023· Northwind Pharmaceuticals LLC

Recalled Item: Glimepiride Tablets Recalled by Northwind Pharmaceuticals LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2023· Northwind Pharmaceuticals LLC

Recalled Item: Tadalafil Tablets Recalled by Northwind Pharmaceuticals LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2023· Northwind Pharmaceuticals LLC

Recalled Item: Atorvastatin Calcium Tablets Recalled by Northwind Pharmaceuticals LLC Due...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 16, 2023· Northwind Pharmaceuticals LLC

Recalled Item: Glimepiride Tablets Recalled by Northwind Pharmaceuticals LLC Due to CGMP...

The Issue: CGMP Deviations

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

Class II — Potential Health HazardOngoing
Refund