State

New Mexico product recalls

72,984 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 72,984 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

5101–5125 of 76609

CriticalFDA (Devices)·Z-2611-2025·2025-10-08
Reprocessed cardiac mapping catheters recalled over residual particulates on device surfaces
Medline is recalling 7,913 reprocessed Webster CS 10-electrode catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Product
Reprocessed Webster CS Catheter 10 Electrodes for electrophysiological mapping of cardiac structures. Medline Item Numbers BD710DF282CRH BD710DF282RRH BD710FJ282CRH BD710FJ282RRH
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2654-2025·2025-10-08
Biograph mMR scanners recalled over ice blockage in magnet venting
Siemens is recalling 27 Biograph mMR systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Product
Biograph mMR. Model Number: 10433372.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2668-2025·2025-10-08
MAGNETOM Vida Fit MRI systems recalled over magnet vent ice blockage
Siemens is recalling 41 MAGNETOM Vida Fit MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Product
MAGNETOM Vida Fit. Model Number: 11410481.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2656-2025·2025-10-08
MAGNETOM Cima.X systems recalled over ice blockage in helium venting system
Siemens is recalling 22 MAGNETOM Cima.X (DE) systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.
Product
MAGNETOM Cima.X (DE). Model Number: 11647158.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2617-2025·2025-10-08
Atlan A350XL anesthesia workstations recalled after piston ventilator failures during use
Draeger is recalling 223 Atlan A350XL anesthesia workstations that either indicated a piston ventilator failure before use or suffered a mechanical ventilation failure during use.
Product
Brand Name: Atlan Product Name: Atlan A350XL Model/Catalog Number: 8621600 Software Version: Not Applicable Product Description: The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neonates. The device can be used for mechanical ve
Category
Medical Device
Distribution
25 states
CriticalFDA (Devices)·Z-2667-2025·2025-10-08
MAGNETOM Vida MRI systems recalled over ice blockage in magnet venting
Siemens is recalling 498 MAGNETOM Vida (DE) MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Product
MAGNETOM Vida (DE). Model Number: 11060815. 510(k): K170396, K173617, K181433, K183254, K192924, K203443, K213693, K213805, K220425, K231560.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2614-2025·2025-10-08
Reprocessed ultrasound catheters recalled over residual particulates on patient contacting surfaces
Medline is recalling 7,913 reprocessed ACUSON AcuNav ultrasound catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Product
Reprocessed ACUSON AcuNav Ultrasound Catheter for intracardiac and intra-luminal visualization of cardiac and great vessel anatomy and physiology as well as visualization of other devices in the heart. For imaging guidance only, not treatment delivery, during cardiac interventio
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2663-2025·2025-10-08
MAGNETOM Spectra MRI systems recalled over helium venting ice blockage
Siemens is recalling three MAGNETOM Spectra MRI systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.
Product
MAGNETOM Spectra as the following: 1. MAGNETOM Spectra. Model Number: 10837643. 2. MAGNETOM Spectra (CN). Model Number: 10655588.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2660-2025·2025-10-08
MAGNETOM Skyra MRI systems recalled over ice blockage in venting system
Siemens is recalling 586 MAGNETOM Skyra (DE) MRI systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.
Product
MAGNETOM Skyra (DE). Model Number: 10432915. 510(k) Numbers: K101347, K111242, K123510, K133435, K140253, K141977, K142515, K153343, K173592, K202014, K231560.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2659-2025·2025-10-08
MAGNETOM Prisma MRI systems recalled over helium venting ice blockage
Siemens is recalling 101 MAGNETOM Prisma MRI systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.
Product
MAGNETOM Prisma. Model Number: 10849582.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2613-2025·2025-10-08
Reprocessed cardiac imaging catheters recalled over residual particulates on device surfaces
Medline is recalling 7,913 reprocessed ViewFlex Xtra ICE catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Product
Reprocessed ViewFlex Xtra ICE Catheter to visualize cardiac structures; blood flow and other devices within the heart. Medline Item Numbers D087031RH
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2658-2025·2025-10-08
MAGNETOM Lumina MRI systems recalled over helium venting ice blockage risk
Siemens is recalling 130 MAGNETOM Lumina (DE) MRI systems because an ice blockage in the magnet venting system could prevent helium escaping during a quench.
Product
MAGNETOM Lumina (DE). Model Number: 11344916.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2610-2025·2025-10-08
Reprocessed steerable electrophysiology catheters recalled over residual particulates on surfaces
Medline is recalling 7,913 reprocessed Livewire Steerable Electrophysiology Catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Product
Reprocessed Livewire Steerable Electrophysiology Catheter Item Numbers 401575RH 401582RH 401600RH 401603RH 401606RH 401652RH 401653RH 401654RH 401904RH 401905RH 401908RH 401914RH 401915RH 401918RH 401932RH 401933RH 401934RH 401938RH 401939RH 401940RH 401941
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2657-2025·2025-10-08
MRI scanner recalled over ice blockage in magnet helium venting system
A MAGNETOM Connectom.X MRI system is being recalled because an ice blockage in the magnet venting system could prevent helium from escaping during a quench.
Product
MAGNETOM Connectom.X. Model Number: 11371480.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2616-2025·2025-10-08
Atlan A350 anesthesia workstations recalled after mechanical ventilation failures were reported
Draeger is recalling 530 Atlan A350 anesthesia workstations that either indicated a piston ventilator failure before use or suffered a mechanical ventilation failure during use.
Product
Brand Name: Atlan Product Name: Atlan A350 Model/Catalog Number: 8211500 Software Version: Not applicable Product Description: The Atlan is an anesthesia workstation intended for use in anesthetizing adults, pediatrics, and neonates. The device can be used for mechanical vent
Category
Medical Device
Distribution
25 states
CriticalFDA (Devices)·Z-2664-2025·2025-10-08
MAGNETOM Verio MRI systems recalled over magnet venting ice blockage risk
Siemens is recalling 154 MAGNETOM Verio MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Product
MAGNETOM Verio. Model Number: 10276755.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2666-2025·2025-10-08
MAGNETOM Verio Dot Upgrade systems recalled over magnet venting ice blockage
Siemens is recalling 78 MAGNETOM Verio Dot Upgrade systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Product
MAGNETOM Verio Dot Upgrade. Model Number: 10684334.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2612-2025·2025-10-08
Reprocessed electrophysiology catheters recalled over residual particulates on patient surfaces
Medline is recalling 7,913 reprocessed Inquiry Steerable Diagnostic Catheters because specific lots may carry small residual particulates on patient-contacting surfaces.
Product
Reprocessed Inquiry Steerable Diagnostics Catheter for electrogram recording and cardiac stimulation during diagnostic electrophysiologic studies; Medline Item Numbers 81102RH 81104RH 81107RH 81174RH 81402RH 81404RH 81405RH 81472RH 81473RH 81474RH 81531RH 81532RH
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2661-2025·2025-10-08
MAGNETOM Skyra fit MRI systems recalled over magnet vent ice blockage
Siemens is recalling 56 MAGNETOM Skyra fit MRI systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Product
MAGNETOM Skyra fit. Model Number: 10849580.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2665-2025·2025-10-08
MAGNETOM Verio Dot systems recalled over magnet venting ice blockage risk
Siemens is recalling 59 MAGNETOM Verio Dot systems because an ice blockage in the magnet venting system could stop helium escaping during a quench.
Product
MAGNETOM Verio Dot. Model Number: 10684333.
Category
Medical Device
Distribution
Distributed nationwide
CriticalFDA (Devices)·Z-2670-2025·2025-10-08
Surgical valve pack kits recalled after cannulas may not retain shape
Medline is recalling 828 VALVE PACK-LF kits because they contain lots of cannula products where the catheter may not retain its shape.
Product
Medline Kits: 1) VALVE PACK-LF, Model Number: DYNJ0415366P; 2) VALVE PACK-LF, Model Number: DYNJ0415366Q
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V671000·2025-10-08
2026 BMW X6 and X4 Vehicles Recalled for Windshield Seal Defect
BMW is recalling 2026 X6 and X4 vehicles because the windshield may not be sealed properly, allowing water to enter electrical components and potentially causing loss of lights, door functions, or fire.
Product
BMW — BMW X4, X6
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V672000·2025-10-08
BMW motorcycles recalled over cardan shaft that may lose drive power
BMW is recalling three 2026 R 1300 RT motorcycles whose cardan shaft may not have been sufficiently hardened, allowing the universal joint to slip and causing a loss of drive power.
Product
BMW — BMW R 1300 RT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25T017000·2025-10-08
Continental Recalls Specific Tires Due to Tread Detachment Risk
Continental is recalling specific tire models because the wrong rubber compound was used, which may cause the tread to detach and increase crash risk.
Product
TIRES:TREAD/BELT recall
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0016-2026·2025-10-08
Washer disinfectors recalled over overheating risk from incorrect pressure calibration
Getinge is recalling 902 88-Series washer-disinfectors that can overheat during operation if the circulation pressure calibration was not performed, or was performed incorrectly.
Product
Getinge 88-Series Washer- Disinfector. Model Number: 88-5.
Category
Medical Device
Distribution
Distributed nationwide