State

New Mexico product recalls

72,940 recalls have nationwide distribution and so reach New Mexico. 3,625 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total: 3,625
Critical: 747
Severe: 647
Most recent: 2026-09-02

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 72,940 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2526–2550 of 76565

HighFDA (Devices)·Z-1694-2026·2026-04-08
Olympus SOLTIVE Premium laser power supply may fail producing smoke
Olympus is recalling SOLTIVE Premium SuperPulsed Laser Systems because a potential defect in the 24V power supply module may render the system inoperable and produce smoke or a burning smell.
Product
Brand Name: Olympus SOLTIVE Premium SuperPulsed Laser System Product Name: SOLTIVE Premium Laser System TFL-PLS Model/Catalog Number: TFL-PLS containing TFL-CPLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1655-2026·2026-04-08
Paradise renal denervation catheter distributed despite being marked for scrapping
Recor Medical is recalling one lot of the Paradise Ultrasound Renal Denervation System Catheter because a nonconforming product that should have been scrapped was distributed instead.
Product
Brand Name: Paradise¿ Ultrasound Renal Denervation System Product Name: Paradise ¿ Catheter Model/Catalog Number: PRDS-068-02 Product Description: Common name: Ablation catheter renal denervation
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1755-2026·2026-04-08
Burlington Medical kilts may lose radiation attenuation over time
Burlington Medical is recalling kilts made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.
Product
Burlington Medical, Kilt
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1702-2026·2026-04-08
VOLT locking screw taps swapped between lots carry incorrect thread
The 2.4 VOLT Tap Locking Screw Tap is being recalled after a full lot swap with the Cortical Screw Tap left the bone taps with an incorrect thread.
Product
2.4 VOLT TAP LOCKING SCREW TAP TO 90MM. Part Number: 03.424.124-US.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1691-2026·2026-04-08
Medline ENFit G-tube connector kits may leak from dimensional defect
Medline is recalling kits containing ENFit G-tube connectors because the connectors were not made to required dimensional specifications and may not form a proper seal.
Product
Medline Kits containing ENFIT G-TUBE CONNECTOR 1. SKU DYKM2720 G/J TUBE CARE KIT 2. SKU ENFITDISCKIT ENFIT DISCHARGE KIT
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1708-2026·2026-04-08
Medline endoscopy kits contain recalled Olympus biopsy valves shedding fragments
Medline is recalling BAL and ENDO kits because they contain recalled Olympus biopsy valves, where rubber fragments may detach from the valve slit during use.
Product
Medline kits containing Olympus biopsy valves: 1. BAL KIT, DYNDA2137B 2. ENDO KIT, DYKE1915
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1747-2026·2026-04-08
MiniMed 620G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 620G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 620G Insulin Pump (MMT-1750)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1756-2026·2026-04-08
Burlington Medical frontal aprons may lose radiation attenuation over time
Burlington Medical is recalling frontal aprons made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.
Product
Burlington Medical, Frontal Aprons
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1764-2026·2026-04-08
Burlington Medical blockers may lose radiation attenuation over time
Burlington Medical is recalling blockers because of the potential for attenuation degradation over time, decreasing the lifespan of the product.
Product
Burlington Medical, Blockers.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0408-2026·2026-04-08
Amneal tramadol tablets failed nitrosamine impurity specification at stability
Amneal Pharmaceuticals is recalling two lots of Tramadol Hydrochloride Tablets 50 mg after a nitrosamine impurity was found out of specification at the 24-month stability interval.
Product
TRAMADOL HYDROCHLORIDE — TRAMADOL HYDROCHLORIDE (TRAMADOL HYDROCHLORIDE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1740-2026·2026-04-08
MiniMed 630G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 630G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 630G Insulin Pump (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1751-2026·2026-04-08
MiniMed 530G insulin pump delivery varies with pump height changes
Medtronic is recalling MiniMed 530G insulin pumps because raising or lowering the pump relative to the infusion site can cause unintended over- or under-delivery of insulin.
Product
MiniMed 530G Insulin Pump (MMT-551, MMT-751)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0410-2026·2026-04-08
Quality Choice moisturizing relief eye drops recalled over sterility assurance
Quality Choice Moisturizing Relief Eye Drops, containing dextran 70, polyethylene glycol 400, povidone and tetrahydrozoline hydrochloride, are being recalled for lack of assurance of sterility.
Product
QUALITY CHOICE MOISTURIZING RELIEF EYE DROPS — QUALITY CHOICE MOISTURIZING RELIEF EYE DROPS (DEXTRAN 70, POLYETHYLENE GLYCOL 400, POVIDONE, TETRAHYDROZOLINE HCL)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1692-2026·2026-04-08
Vue Motion V12 may display cine image frames out of sequence
Philips is recalling Vue Motion V12 because mis-ordered frames during dynamic cine runs may cause image frames to display out of sequence.
Product
Vue Motion V12. Product Number: 1017979.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1693-2026·2026-04-08
Sterile radiology procedure kits may have a breached sterile pouch
One lot of Sterile Radiology Procedure Kits, model DYNDH1491B, is being recalled because of a potential breach in the sterile pouch packaging that may compromise sterility.
Product
Sterile Radiology Procedure Kits, Model Number DYNDH1491B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1754-2026·2026-04-08
Burlington Medical radiation protection vests may lose attenuation over time
Burlington Medical is recalling protective vests because of the potential for attenuation degradation over time, decreasing the lifespan of the garment.
Product
Burlington Medical, Vest
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0416-2026·2026-04-08
Leader artificial tears 15 mL recalled over sterility assurance failure
Leader Artificial Tears 15 mL, containing polyvinyl alcohol and povidone, are being recalled for lack of assurance of sterility.
Product
LEADER ARTIFICIAL TEARS 15 ML — LEADER ARTIFICIAL TEARS 15 ML (POLYVINYL ALCOHOL, POVIDONE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0411-2026·2026-04-08
Artificial tears glycerin drops recalled over lack of sterility assurance
Artificial Tears containing glycerin are being recalled for lack of assurance of sterility. About 1,023,096 bottles were distributed nationwide.
Product
ARTIFICIAL TEARS — ARTIFICIAL TEARS (GLYCERIN)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1765-2026·2026-04-08
Burlington Medical kilt blockers may lose radiation attenuation over time
Burlington Medical is recalling kilt blockers because of the potential for attenuation degradation over time, decreasing the lifespan of the product.
Product
Burlington Medical, Kilt Blockers.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1767-2026·2026-04-08
GE SIGNA Premier MRI magnets may have ferrous fittings fitted
SIGNA Premier MRI systems are being recalled because they may have been built or serviced with ferrous steel fittings instead of non-ferrous brass on the magnet rear.
Product
SIGNA Premier systems
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1707-2026·2026-04-08
Medline thoracic robot kits contain recalled Olympus biopsy valves
Medline is recalling Thoracic Robots kits, model DYNJ908777B, because they contain recalled Olympus biopsy valves where rubber fragments may detach from the valve slit.
Product
THORACIC ROBOTS, DYNJ908777B
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1759-2026·2026-04-08
Burlington Medical protective sleeves may lose radiation attenuation over time
Burlington Medical is recalling protective sleeves made with Xenolite 800 attenuation material because of the potential for attenuation degradation over time.
Product
Burlington Medical, Protective Sleeves.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1695-2026·2026-04-08
Olympus SOLTIVE Pro laser power supply may fail producing smoke
Olympus is recalling SOLTIVE Pro SuperPulsed Laser Systems because a potential defect in the 24V power supply module may render the system inoperable and produce smoke or a burning smell.
Product
Brand Name: Olympus SOLTIVE Pro SuperPulsed Laser System Product Name: SOLTIVE Pro Laser System TFL-SLS Model/Catalog Number: TFL-SLS containing TFL-CSLU Product Description: An electricity powered device assembly which emits a high-power laser beam to vaporize/ablate soft tis
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1701-2026·2026-04-08
da Vinci permanent cautery hook recalled over frayed pitch cables
Intuitive Surgical is recalling da Vinci S and Si Permanent Cautery Hook Instruments following increased complaints regarding frayed or broken pitch cables on reusable surgical instruments.
Product
Brand Name: da Vinci S, Si Permanent Cautery Hook Instrument Product Name: da Vinci S, Si Permanent Cautery Hook Instrument Model/Catalog Number: 420183 Software Version: NA Product Description: EndoWrist Instruments or da Vinci S/Si Reusable instruments, including blunt and
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1690-2026·2026-04-08
Medline ENFit G-tube connectors may leak from dimensional specification failure
Medline is recalling ENFit G-tube connectors because they were not manufactured to required dimensional specifications and may not form a proper seal with ENFit-style devices.
Product
ENFIT G-TUBE CONNECTOR, MEDLINE Item No. ENFIT1010GC
Category
Medical Device
Distribution
Distributed nationwide