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. 2,542 recalls have been distributed to New Mexico in the last 12 months.

48,595 total recalls
2,542 in last 12 months

Showing 92619280 of 48,595 recalls

DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Megestrol Acetate Oral Suspension Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Ferrous Sulfate Iron Supplement Drops Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Artificial Tears Solution Recalled by Akorn, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Apotex Corp.

Recalled Item: Calcitonin Salmon (synthetic origin) Nasal Spray Recalled by Apotex Corp....

The Issue: Presence of Foreign Substance: Glass splinter particle entrapped inside the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Olopatadine HCl Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Clobetasol Propionate Ointment Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Rifampin Capsules USP Recalled by Akorn, Inc. Due to CGMP Deviations: Firm...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Ephedrine Sulfate Injection Recalled by Akorn, Inc. Due to CGMP Deviations:...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Gadget Island, Inc

Recalled Item: DYNAMITE SUPER capsule Recalled by Gadget Island, Inc Due to Undeclared...

The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 26, 2023· Gadget Island, Inc

Recalled Item: Pro Power Knight Plus capsule Recalled by Gadget Island, Inc Due to...

The Issue: Marketed without an Approved NDA/ANDA: FDA analysis found product to be...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Ropivacaine Hydrochloride Injection USP Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: Atropine Sulfate Ophthalmic Solution Recalled by Akorn, Inc. Due to CGMP...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 26, 2023· Akorn, Inc.

Recalled Item: AK-POLY-BAC (bacitracin Zinc and Polymyxin B Sulfate) Ophthalmic Ointment...

The Issue: CGMP Deviations: Firm went out of business and could no longer continue...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 26, 2023· HeartSine Technologies Ltd

Recalled Item: HeartSine Recalled by HeartSine Technologies Ltd Due to Single use battery...

The Issue: Single use battery and electrode cartridge may be rendered inoperable due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Davol, Inc.

Recalled Item: Ventralight ST 4" x 6" Ellipse with Echo PS Catalog Number: 5955460 Recalled...

The Issue: Balloon may not inflate as intended. If the balloon does not inflate during...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· LumiraDx

Recalled Item: SteriPack Sterile Polyester Spun Swabs (25 units/Pack)- Intended for sample...

The Issue: Fails Post-Sterilization Sterile Swabs Cantilever (Bend) Testing and may be...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Philips North America

Recalled Item: Incisive CT for Brazil SKD-Computed Tomography X-Ray System Model: 728146...

The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Philips North America

Recalled Item: Incisive CT-Computed Tomography X-Ray System Model: 728143 Recalled by...

The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Linkbio Corp.

Recalled Item: LINK SymphoKnee System L-Shaped Femoral Augment Recalled by Linkbio Corp....

The Issue: Contains the incorrect implant in the packaging. The packaging incorrectly...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 25, 2023· Philips North America

Recalled Item: Incisive CT Power (China)-Computed Tomography X-Ray System Model: 728148...

The Issue: Metal mounting box on the rotating scanner on rotor (heat exchanger box)...

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

Class II — Potential Health HazardOngoing