State
73,806 recalls have nationwide distribution and so reach New Mexico. 3,638 additional recalls listed New Mexico specifically in their distribution scope.
Of the 3,638 recalls naming New Mexico we have scored against our rubric, 745 (20%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 816 (22%) are Severe.
Which agencies issued them
These figures cover only the 3,638 recalls whose distribution notice names New Mexico specifically. The 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.
Herbal Doctor Remedies is recalling Glauco-Catar Capsules because they were manufactured outside of current Good Manufacturing Practices controls.
Herbal Doctor Remedies is recalling Stomach Flu Capsules because they were manufactured outside of required Good Manufacturing Practices controls.
Herbal Doctor Remedies is recalling Asma Aid because it was manufactured outside of required Good Manufacturing Practices. The product was distributed nationwide and in Brazil.
Herbal Doctor Remedies is recalling Anemia Off because it was manufactured outside of required Good Manufacturing Practices. The product was distributed nationwide in the US and Brazil.
Herbal Doctor Remedies is recalling Prostatin Capsules because they were manufactured outside of current Good Manufacturing Practice controls.
Herbal Doctor Remedies is recalling Lipidtrol Capsules because they were manufactured outside of current Good Manufacturing Practices controls.
Ortho Clinical Diagnostics is recalling 30 VITROS 250AT Chemistry Systems due to a software anomaly that may cause unsuccessful calibration.
Ortho Clinical Diagnostics is recalling 30 VITROS 350 Chemistry Systems due to a software anomaly that may cause unsuccessful calibration.
Ortho Clinical Diagnostics is recalling 825 VITROS 4600 Chemistry Systems worldwide due to a software anomaly that may cause unsuccessful calibrations.
Philips is recalling 25 IQon Spectral CT systems because cardiac images may be incorrectly labeled as having phase tolerance applied when it was not.
Herbal Doctor Remedies is recalling Mental Tonic Capsules because they were manufactured outside of current Good Manufacturing Practice controls.
Herbal Doctor Remedies is recalling Edema Off Capsules because they were manufactured outside of current Good Manufacturing Practices (CGMP) controls.
Ortho Clinical Diagnostics is recalling VITROS 5,1 FS Chemistry Systems due to a software anomaly that may cause unsuccessful calibrations.
Howmedica Osteonics Corp. is recalling 11 Serrato polyaxial screws because some 90mm and 100mm units were manufactured with the wrong length.
Glenmark Pharmaceuticals is recalling Mometasone Furoate Cream 0.1% because patients reported the product felt gritty. The recall covers 15g and 45g tubes distributed nationwide.
Herbal Doctor Remedies is recalling Lung Saver Capsules because they were manufactured outside of current Good Manufacturing Practices controls.
Ortho Clinical Diagnostics is recalling VITROS Chemistry Products Calibrator Kit 32 due to a software anomaly that may cause unsuccessful calibration.
Philips is recalling 128 iCT computed tomography systems because cardiac images may be incorrectly labeled as having phase tolerance applied when it was not.
RXQ Compounding LLC is recalling Ascorbic Acid 400 MG/ML Injection Solution because of crystallization. The recall covers all lots within expiry distributed nationwide.
American Health Packaging is recalling 14,360 bottles of Lovastatin 40 mg tablets because the drug substance was out of specification for impurity results.
Biomet 3i is recalling 17 units of Certain Bellatek Titanium Abutments because a manufacturing defect prevents the screw from seating correctly.
Herbal Doctor Remedies is recalling Awake 500 mg capsules because they were manufactured outside of required Good Manufacturing Practices.
Herbal Doctor Remedies is recalling Bone Fixer because it was manufactured outside of required Good Manufacturing Practices controls.
Mott's LLP is recalling Penafiel Mineral Spring Water bottles because of elevated levels of inorganic arsenic. The recall covers 62,349 cases distributed nationwide.
Philips is recalling Azurion interventional fluoroscopic X-ray systems because a cold restart may take up to 7 minutes, potentially delaying treatment.