State

New Mexico product recalls

73,833 recalls have nationwide distribution and so reach New Mexico. 3,638 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total: 3,638
Critical: 745
Severe: 816
Most recent: 2026-11-04

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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

41501–41525 of 77471

SevereFDA (Devices)·Z-0585-2018·2018-02-28
Medtronic Recalls 951 Evera MRI ICDs Due to Therapy Prevention Risk
Medtronic is recalling 951 Evera MRI ICDs and CRT-Ds because a defect may prevent high and low voltage therapy. Patients should contact their healthcare provider.
Product
Implantable Cardioverter Defibrillators (ICDs), Evera MRI. Labeled as the following: a. Evera MRI XT DR ICD DF1 (Product No. DDMB1D1); b. Evera MRI XT DR ICD DF4 (Product No. DDMB1D4); c. Evera MRI XT VR ICD DF4 (Product No. DVMB1D4); d. Evera MRI S DR ICD DF1…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0432-2018·2018-02-28
Pharmedium Recalls Ephedrine Sulfate Injection Due to Sterility Concerns
Pharmedium Services, LLC is recalling Ephedrine Sulfate in 0.9% Sodium Chloride nationwide due to a lack of sterility assurance.
Product
Ephedrine Sulfate in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0456-2018·2018-02-28
Pharmedium Recalls Atropine Sulfate Injection Due to Sterility Concerns
Pharmedium Services, LLC is recalling all lots of Atropine Sulfate Injection nationwide due to a lack of sterility assurance.
Product
Atropine Sulfate Injection in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0431-2018·2018-02-28
Pharmedium Recalls Fentanyl and Bupivacaine Injections Due to Sterility Concerns
Pharmedium Services, LLC is recalling Fentanyl Citrate and Bupivacaine HCl injections due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.
Product
Fentanyl Citrate and Bupivacaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0449-2018·2018-02-28
Pharmedium Recalls Midazolam HCl Injection Due to Sterility Concerns
Pharmedium Services, LLC is recalling all lots of Midazolam HCl Injection because of a lack of sterility assurance. The recall covers all strengths, doses, and packaging distributed nationwide.
Product
Midazolam HCl Injection in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0537-2018·2018-02-28
FDA Recalls Methylcobalamin Due to Missing Stability Data
American Pharmaceutical Ingredients LLC is recalling Methylcobalamin (Vitamin B12) for prescription compounding because the manufacturer lacked stability data to support the assigned expiration dates.
Product
Methylcobalamin (Vitamin B12) for prescription compounding, packaged in a) 500mg (NDC 58597-8142-1); b) 1g (NDC 58597-8056-2); c) 5g (NDC 58597-8056-3); d) 10g (NDC 58597-8056-4), e) 25 g (NDC 58597-8056-4); f) 100g (NDC 58597-8056-6), RX only, packed by American Pharmaceutical…
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0586-2018·2018-02-28
Medtronic Recalls Claria MRI CRT-Ds Due to Therapy Prevention Risk
Medtronic is recalling 951 Claria MRI CRT-Ds because a defect may prevent the devices from delivering high or low voltage therapy.
Product
Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), Claria MRI. Labeled as the following: a. Claria MRI CRT-D DF1 (Product No. DTMA1D1); b. Claria MRI Quad CRT-D DF4 (Product No. DTMA1QQ); EXPANSION: c. Claria MRI CRT-D DF4 (Product No. DTMA1D4); d.…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0448-2018·2018-02-28
Pharmedium Recalls Methadone HCl Injection Due to Sterility Concerns
Pharmedium Services, LLC is recalling all lots of Methadone HCl in 0.9% Sodium Chloride due to a lack of sterility assurance.
Product
Methadone HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0428-2018·2018-02-28
Pharmedium Recalls Hydromorphone HCl Injection Due to Sterility Concerns
Pharmedium Services, LLC is recalling all lots of Hydromorphone HCl in Sodium Chloride 0.9% due to a lack of sterility assurance.
Product
HYDROmorphone HCl in Sodium Chloride 0.9% in all doses, all strengths, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0445-2018·2018-02-28
Pharmedium Recalls Phenylephrine HCl Injections Due To Sterility Concerns
Pharmedium Services, LLC is recalling all lots of Phenylephrine HCl in 0.9% Sodium Chloride due to a lack of sterility assurance.
Product
Phenylephrine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0462-2018·2018-02-28
Pharmedium Recalls Vecuronium Bromide Injection Due to Sterility Concerns
Pharmedium Services, LLC is recalling Vecuronium Bromide in Sterile Water for Injection due to a lack of sterility assurance. The recall covers all lots remaining within expiry nationwide.
Product
Vecuronium Bromide in Sterile Water for Injection in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0467-2018·2018-02-28
Pharmedium Recalls Rocuronium Bromide Due to Sterility Assurance Concerns
Pharmedium Services, LLC is recalling all Rocuronium Bromide products due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.
Product
Rocuronium Bromide in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0436-2018·2018-02-28
Pharmedium Recalls Morphine Sulfate Injection Due to Sterility Concerns
Pharmedium Services, LLC is recalling all lots of Morphine Sulfate in 0.9% Sodium Chloride nationwide due to a lack of sterility assurance.
Product
Morphine Sulfate in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0442-2018·2018-02-28
Pharmedium Recalls Succinylcholine Chloride Due to Sterility Assurance Concerns
Pharmedium Services, LLC is recalling all strengths and doses of Succinylcholine Chloride due to a lack of sterility assurance.
Product
Succinylcholine Chloride in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0435-2018·2018-02-28
Pharmedium Recalls Midazolam HCl in 5% Dextrose Due to Sterility Concerns
Pharmedium Services, LLC is recalling all lots of Midazolam HCl in 5% Dextrose due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.
Product
Midazolam HCl in 5% Dextrose in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0589-2018·2018-02-28
Medtronic Visia AF ICDs Recalled for Potential Therapy Failure
Medtronic is recalling 951 Visia AF ICDs and CRT-Ds because they may fail to deliver high or low voltage therapy.
Product
Implantable Cardioverter Defibrillators (ICDs), Visia AF. Labeled as: a. Visia AF VR ICD DF1 (Product No. DVAB1D1); EXPANSION: b. Visia AF" VR ICD DF4 (Product No. DVAB1D4) Implantable devices that automatically detect and treat episodes of ventricular…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0446-2018·2018-02-28
Pharmedium Recalls Potassium Chloride in 5% Dextrose Due to Sterility Concerns
Pharmedium Services, LLC is recalling all lots of Potassium Chloride in 5% Dextrose due to a lack of sterility assurance. The recall covers all strengths, doses, and packaging nationwide.
Product
Potassium Chloride in 5% Dextrose in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0454-2018·2018-02-28
Pharmedium Recalls Glycopyrrolate Due to Lack of Sterility Assurance
Pharmedium Services, LLC is recalling all strengths and packaging of Glycopyrrolate due to a lack of sterility assurance. The recall covers all lots remaining within their expiry dates nationwide.
Product
Glycopyrrolate in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0457-2018·2018-02-28
Pharmedium Recalls Hydromorphone HCl in 5% Dextrose Due to Sterility Concerns
Pharmedium Services, LLC is recalling Hydromorphone HCl in 5% Dextrose in all strengths and packaging due to a lack of sterility assurance.
Product
HYDROmorphone HCl in 5% Dextrose in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0452-2018·2018-02-28
Pharmedium Recalls Ketamine HCl Injection Due to Sterility Assurance Concerns
Pharmedium Services, LLC is recalling all lots of Ketamine HCl Injection because of a lack of sterility assurance. The recall covers all strengths, doses, and packaging distributed nationwide.
Product
Ketamine HCl Injection in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0640-2018·2018-02-28
GastriSail Gastric Positioning Device Recalled Due to Perforation Reports
FDA is recalling 17,271 units of the GastriSail Gastric Positioning Device due to reports of gastric or esophageal perforation during surgical procedures.
Product
GastriSail" Gastric Positioning Device Product Usage: The GastriSail gastric positioning system is indicated for use in gastric and bariatric surgical procedures for the application of suction, decompression and to radially expand the stomach, to drain gastric fluids, to test…
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0440-2018·2018-02-28
Pharmedium Recalls Potassium Chloride Infusions Due to Sterility Concerns
Pharmedium Services, LLC is recalling all lots of Potassium Chloride in 0.9% Sodium Chloride due to a lack of sterility assurance.
Product
Potassium Chloride in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0430-2018·2018-02-28
Pharmedium Recalls Fentanyl and Ropivacaine Injection Due to Sterility Concerns
Pharmedium Services, LLC is recalling Fentanyl Citrate and Ropivacaine HCl injections because of a lack of sterility assurance. The recall covers all lots remaining within their expiry dates nationwide.
Product
Fentanyl Citrate and Ropivacaine HCl in 0.9% Sodium Chloride in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Drugs)·D-0450-2018·2018-02-28
Pharmedium Recalls Fentanyl Citrate Injection Due to Sterility Concerns
Pharmedium Services, LLC is recalling Fentanyl Citrate Injection in all strengths and packaging due to a lack of sterility assurance.
Product
Fentanyl Citrate Injection in all strengths, all doses, and all packaging.
Category
Drug
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-0584-2018·2018-02-28
Medtronic Viva CRT-D Recall for Possible Prevention of Therapy
Medtronic is recalling 951 Viva CRT-D devices due to a potential issue that may prevent high and low voltage therapy.
Product
Cardiac Resynchronization Therapy Defibrillators (CRT-Ds), Viva. Labeled as the following: a. Viva Quad S CRT-D DF4 (Product No. DTBB1QQ); b. Viva Quad XT CRT-D DF4 (Product No. DTBA1QQ); c. Viva S CRT-D DF1 (Product No. DTBB1D1); d. Viva XT CRT-D DF1 (Product No.…
Category
Medical Device
Distribution
Distributed nationwide