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. 2,579 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,579 in last 12 months

Showing 60216040 of 48,595 recalls

Medical DeviceMarch 27, 2024· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...

The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 27, 2024· Cardinal Health 200, LLC

Recalled Item: Jackson-Pratt 3-Spring Reservoir Kit with PVC Round Drain Recalled by...

The Issue: Cardinal Health is issuing a lot number specific voluntary removal of...

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

Class II — Potential Health HazardOngoing
DrugMarch 26, 2024· Cipla USA, Inc.

Recalled Item: Ipratropium Bromide and Albuterol Sulfate Inhalation Solution USP Recalled...

The Issue: Short fill: Complaints received of less fill volume in respule and few drops...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 26, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Diltiazem Hydrochloride Extended-Release Capsules Recalled by Glenmark...

The Issue: Failed Dissolution Specifications: Out of Specification (OOS) was reported...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 26, 2024· Philips Respironics, Inc.

Recalled Item: BiPAP V30 Auto Ventilator Recalled by Philips Respironics, Inc. Due to...

The Issue: Potential for devices to experience interruption/loss of therapy during a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2024· Philips Respironics, Inc.

Recalled Item: BiPAP A40 Ventilators: BiPAP A40 Recalled by Philips Respironics, Inc. Due...

The Issue: Potential for devices to experience interruption/loss of therapy during a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2024· Philips Respironics, Inc.

Recalled Item: BiPAP A30 Ventilator Recalled by Philips Respironics, Inc. Due to Potential...

The Issue: Potential for devices to experience interruption/loss of therapy during a...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 26, 2024· Medtronic Navigation, Inc.

Recalled Item: Stealth S8 Clinical Software Application Recalled by Medtronic Navigation,...

The Issue: Due to a software issue, there is the potential for a missing digit, letter,...

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

Class I — Serious Health HazardOngoing
DrugMarch 25, 2024· Amneal Pharmaceuticals of New York, LLC

Recalled Item: Methylergonovine Maleate Tablets Recalled by Amneal Pharmaceuticals of New...

The Issue: Failed Dissolution Specifications

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 25, 2024· Novitium Pharma LLC

Recalled Item: Digoxin Tablets Recalled by Novitium Pharma LLC Due to Failed...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKN130002 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKNXC0005 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKNXC0003 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 25, 2024· Ossur H / F

Recalled Item: RKN130003 Recalled by Ossur H / F Due to Due to firmware issues with the...

The Issue: Due to firmware issues with the prosthetic knee, there is the potential for...

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

Class II — Potential Health HazardOngoing
DrugMarch 23, 2024· Aruba Aloe Balm N.V.

Recalled Item: Alcoholada Gel Recalled by Aruba Aloe Balm N.V. Due to Chemical...

The Issue: Chemical Contamination: Product manufactured with ethanol API that contains...

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

Class I — Serious Health HazardOngoing
Refund
DrugMarch 23, 2024· Aruba Aloe Balm N.V.

Recalled Item: Aruba Aloe Hand Sanitizer Gel Recalled by Aruba Aloe Balm N.V. Due to...

The Issue: Chemical Contamination: Product manufactured with ethanol API that contains...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMarch 23, 2024· Philips Ultrasound, Inc.

Recalled Item: 5000 Compact Series Ultrasound Systems Recalled by Philips Ultrasound, Inc....

The Issue: Ultrasound system with: 1) transesophageal echocardiography transducer (TEE)...

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

Class II — Potential Health HazardOngoing
FoodMarch 22, 2024· Pepsico Inc.

Recalled Item: 12 oz Aluminum cans of root beer packaged 12 cans per carton. 2/12pks per...

The Issue: Product was mislabeled. Can labeled as regular Mug contains Mug Zero Sugar

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2024· IntegraDose Compounding Services LLC

Recalled Item: fentaNYL Citrate 2 Recalled by IntegraDose Compounding Services LLC Due to...

The Issue: Lack of Assurance of Sterility: leaking bags

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2024· B. Braun Medical Inc

Recalled Item: Lactated Ringer's Injection USP Recalled by B. Braun Medical Inc Due to Lack...

The Issue: Lack of assurance of sterility: bags have the potential to leak..

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

Class II — Potential Health HazardOngoing
Refund