State
72,936 recalls have nationwide distribution and so reach New Mexico. 3,625 additional recalls listed New Mexico specifically in their distribution scope.
Of the 3,625 recalls naming New Mexico we have scored against our rubric, 747 (21%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 647 (18%) are Severe.
Which agencies issued them
These figures cover only the 3,625 recalls whose distribution notice names New Mexico specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Zydus Pharmaceuticals is recalling Erythromycin Tablets, 250 mg, nationwide because certain lots contain N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit due to CGMP deviations.
Blackstone Parmesan Ranch Seasoning in 7.3 oz containers is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.
PS Seasoning 1P Original Smokehouse Unit is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination. 5,375.6 lbs are affected.
Southern Style Nuts Hunter Mix in 30 oz plastic jars is being recalled over the potential presence of Salmonella. 30,515 cases are affected.
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94725), a cardiopulmonary bypass catheter, because the sterile barrier may be breached, potentially allowing contamination. The cannulas were distributed worldwide.
Ellsworth Sour Cream + Onion Seasoning from PS Seasoning is being recalled because it was made with milk powder recalled by the supplier over Salmonella contamination.
Becton, Dickinson and Company is recalling multiple models of Swan-Ganz Catheters due to potential leaking or breaking of the proximal injectate lumen hub that could lead to infection, medication loss, or blood loss.
Wisconsin Pharmacal Company is recalling MG217 Multi-Symptom Treatment Cream & Skin Protectant due to confirmed presence of Staphylococcus aureus contamination. Affected units are 6 oz tubes with Lot #1024088, expiring 11/30/2026, distributed nationwide and in the Bahamas.
Zydus Pharmaceuticals is recalling erythromycin 500 mg tablets nationwide due to the presence of N-Nitroso-Desmethyl-Erythromycin above the recommended acceptable intake limit, resulting from manufacturing deviations.
Good & Gather Mexican Street Corn Trail Mix in 8 oz bags is being recalled over the potential presence of Salmonella. 272 cases are affected.
Lupin Pharmaceuticals is recalling Liraglutide Injection due to the presence of white thread-like structures (particulate matter) found in cartridges. The recall affects 217,621 pen injectors distributed nationwide.
Medtronic Perfusion Systems is recalling certain lots of the DLP Retrograde Cannula (Model 94913), a cardiopulmonary bypass vascular catheter, due to a potential sterile barrier breach.
Toyota is recalling certain Lexus UX Hybrid, Lexus GX, Toyota Mirai and Land Cruiser Hybrid vehicles because the instrument panel cluster may fail to display certain warnings or indicators.
ICU Medical is recalling Oncology Kits with extension sets due to potential leaks that could interrupt chemotherapy infusion and expose hazardous substances to patients, caregivers, and pharmacy technicians.
Ford is recalling certain 2021–2026 Bronco Sport and 2022–2026 Maverick vehicles due to potentially loose or improperly installed front lower control arm ball joints that could disconnect from the wheel knuckle, risking loss of vehicle control and crashes.
VitaminAlly Liposomal Women's Liquid Multivitamin Drops with Iron are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.
The deaeration hose in Philips Azurion X-ray tube cooling units may degrade over time and leak oil, affecting cooling performance and automatically triggering low-dose fluoroscopy mode.
VitaminAlly Joint Nourish oral liquid is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen contamination and possible C. botulinum concerns.
Medtronic is recalling certain lots of its DLP Retrograde Cannula (Model 94915), a cardiopulmonary bypass vascular catheter, due to potential sterile barrier breach.
Philips is recalling Integris-Allura X-ray systems because deaeration hoses in X-ray tube cooling units may degrade, causing oil leakage that reduces cooling performance and triggers a system shutdown to low-dose mode.
VitaminAlly Liposomal D3+B12 Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
VitaminAlly Liposomal D3-5000IU Spray is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.
VitaminAlly Liposomal Mens Liquid Multivitamin Drops are being recalled over cGMP deviations that could lead to bacterial pathogen and possible C. botulinum concerns.
Medtronic is recalling certain lots of GUNDRY Retrograde Cannula (Model 94113T), a cardiopulmonary bypass catheter, due to potential sterile barrier breach in the product.
VitaminAlly FulviLife Complex oral liquid is being recalled over deviations from current Good Manufacturing Practices that could lead to bacterial pathogen and possible C. botulinum concerns.