State

New Mexico product recalls

73,741 recalls have nationwide distribution and so reach New Mexico. 3,636 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total: 3,636
Critical: 745
Severe: 815
Most recent: 2026-10-28

Of the 3,636 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 815 (22%) are Severe.

Which agencies issued them

These figures cover only the 3,636 recalls whose distribution notice names New Mexico specifically. The 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33626–33650 of 77377

HighFDA (Devices)·Z-2402-2019·2019-09-04
Siemens SOMATOM go.All CT Scanner Recall for Falling Injector Holder
Siemens is recalling 10 SOMATOM go.All CT scanners because the injector holder could fall off. The units are distributed in 20 US states.
Product
SOMATOM go.All; Models #11061630 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·19778·2019-09-04
John Deere Recalls Frontier Grooming Mowers Due to Entanglement Hazard
John Deere is recalling Frontier grooming mowers because incorrect driveline assembly can prevent the safety shield from spinning, posing an entanglement injury risk.
Product
Frontier FM3012, GM1060, GM1072, GM1084, GM1190, GM3060, and GM3072 grooming mowers
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2393-2019·2019-09-04
Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage
Bard Peripheral Vascular Inc is recalling 91 units of GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Product
GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397310, 14.5F, straight, 31cm length, BARD, UDI: 00801741012327
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2384-2019·2019-09-04
Bard Hemodialysis Catheter Recalled for Molded Tip Breakage During Placement
Bard Peripheral Vascular Inc is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during the placement procedure.
Product
GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393230, 14.5F, Straight, 23cm length, BARD, UDI: 00801741012181
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2394-2019·2019-09-04
Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage
Bard Peripheral Vascular Inc is recalling 39 units of GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Product
GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397350, 14.5F, straight, 35cm length, BARD, UDI: 00801741012334
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2381-2019·2019-09-04
Bard Equistream XK Hemodialysis Catheter Recalled for Tip Defect
Bard Peripheral Vascular Inc is recalling 2 units of Equistream XK hemodialysis catheters because the molded tip may break or be damaged during placement.
Product
EQUISTREAM XK Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5913310, 16F, Straight, 31cm length, BARD, UDI: 00801741013867
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2391-2019·2019-09-04
Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage
Bard Peripheral Vascular Inc is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Product
GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397230, 14.5F, straight, 23cm length, BARD, UDI: 00801741012303
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2376-2019·2019-09-04
Bard Equistream XK Hemodialysis Catheter Recalled for Tip Breakage
Bard Peripheral Vascular Inc is recalling Equistream XK Alphacurve Long-Term Hemodialysis Catheters because the molded tip may break or become damaged during placement.
Product
EQUISTREAM XK Alphacurve Long-Term Hemodialysis Catheter REF/Product code:5915240, 16F, 24cm length, BARD, UDI: 00801741013904
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2369-2019·2019-09-04
Bard Equistream Hemodialysis Catheter Recalled for Tip Breakage
Bard Peripheral Vascular Inc is recalling 135 units of Equistream Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Product
EQUISTREAM LONG-TERM HEMODIALYSIS CATHETER, REF/Product code:5905240, 14.5 Fr. Alphacurve Catheter with Standard Kit, 24cm length, BARD, UDI# 00801741013805
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2400-2019·2019-09-04
Siemens SOMATOM go.Up CT Systems Recalled for Falling Injector Holder
Siemens is recalling 18 SOMATOM go.Up CT systems because the injector holder could fall off, posing a risk of injury.
Product
SOMATOM go.Up; Models #11061620 Product Usage: This computed tomography system is intended to generate and process cross-sectional images of patients by computer reconstruction of x-ray transmission data
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2390-2019·2019-09-04
Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage
Bard Peripheral Vascular Inc is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or become damaged during placement.
Product
GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397190, 14.5F, straight, 19cm length, BARD, UDI: 00801741012297
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2387-2019·2019-09-04
Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage
Bard Peripheral Vascular Inc is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or become damaged during placement.
Product
GlidePath Long-Term Hemodialysis Catheter, REF/Product code:5396190, 14.5F, Alphacurve, 19cm length, BARD, UDI: 00801741012242
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2392-2019·2019-09-04
Bard GlidePath Hemodialysis Catheter Recall Due to Tip Damage
Bard Peripheral Vascular Inc is recalling 887 units of GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Product
GlidePath Long-Term Hemodialysis Catheter with Preloaded stylet, REF/Product code:5397270, 14.5F, straight, 27cm length, BARD, UDI: 00801741012310
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2385-2019·2019-09-04
Bard GlidePath Hemodialysis Catheter Recalled for Tip Breakage
Bard Peripheral Vascular Inc is recalling GlidePath Long-Term Hemodialysis Catheters because the molded tip may break or become damaged during placement.
Product
GlidePath Long-Term Hemodialysis Catheter with Preloaded Stylet, REF/Product code:5393270, 14.5F, Straight, 27cm length, BARD, UDI: 00801741012198
Category
Medical Device
Distribution
53 states
HighFDA (Devices)·Z-2374-2019·2019-09-04
Bard Equistream Hemodialysis Catheter Recalled for Molded Tip Defect
Bard Peripheral Vascular Inc is recalling 13 units of Equistream Long-Term Hemodialysis Catheters because the molded tip may break or be damaged during placement.
Product
EQUISTREAM Long-Term Hemodialysis Catheter with Preloaded Styet, REF/Product code:5903310, 14.5F, Straight ,31cm length, BARD, UDI: 00801741013720
Category
Medical Device
Distribution
53 states
ModerateFDA (Devices)·Z-2423-2019·2019-09-04
Stryker Endotrac Hook Blade Recalled for Compromised Sterile Bag Seal
Stryker GmbH is recalling 110 units of Endotrac EPF/EGR Hook Blades because the sterile bag seal integrity may be compromised.
Product
Endotrac EPF/EGR Hook Blade, Angled, Catalog Number 3055A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2414-2019·2019-09-04
Stryker Endotrac ECTR Triangle Blade Recalled Due to Compromised Sterile Bag Seal
Stryker GmbH is recalling 53 Endotrac ECTR Triangle Blades because the sterile bag seal may be compromised, potentially affecting sterility.
Product
Endotrac ECTR Triangle Blade, Catalog Number 2054-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2424-2019·2019-09-04
Stryker Recalls Endintrak 2 Hook Blade Kits Due to Seal Integrity
Stryker GmbH is recalling 259 Endintrak 2 Hook Blade kits because the sterile bag seal integrity may be compromised, potentially affecting sterility.
Product
Endintrak¿ 2 Hook Blade, Angled, Catalog Number 4058A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2415-2019·2019-09-04
Stryker Recalls Endotrac ECTR Hook Blades Due to Seal Integrity Concerns
Stryker GmbH is recalling 1,959 Endotrac ECTR Hook Blades because the sterile bag seal may be compromised, potentially affecting sterility.
Product
Endotrac ECTR Hook Blade, Catalog Number 2055-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2408-2019·2019-09-04
Ad-Tech Skull Anchor Bolts Recalled for Incorrect MRI Approval Labeling
Ad-Tech Medical Instrument Corporation is recalling Skull Anchor Bolts because supplemental information incorrectly indicated they were approved for use in the MR environment.
Product
Skull Anchor Bolts
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2396-2019·2019-09-04
Ad-Tech Spencer Probe Depth Electrodes Recalled for Incorrect Contact Count Labeling
Ad-Tech Medical Instrument Corporation is recalling 18 Spencer Probe Depth Electrodes because two units labeled as 8-contact were actually 6-contact. No patient impact was reported.
Product
AD-TECH Spencer Probe Depth Electrode Product Usage: The Ad-Tech Depth Electrodes (Depth Electrodes, Foramen Ovale Depth Electrodes, Macro Micro Depth Electrodes, Spencer Probe Depth Electrodes, Wyler Sphenoidal Depth Electrodes) are intended for temporary (< 30 days) use…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2406-2019·2019-09-04
Ad-Tech Medical Recalls Subdural Electrodes Due to Incorrect MR Safety Labeling
Ad-Tech Medical Instrument Corporation is recalling subdural electrodes because supplemental information incorrectly stated they were approved for use in MRI environments.
Product
Dual-Sided Interhemispheric, Grid, Intraoperative, Strip, Wyler Subdural Electrodes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2420-2019·2019-09-04
Stryker Recalls Endotrac ECTR Triangle Blades Due to Seal Integrity
Stryker GmbH is recalling 94 Endotrac ECTR Triangle Blades because the sterile bag seal may be compromised, potentially affecting sterility.
Product
Endotrac ECTR Triangle Blade, Angled, Catalog Number 2054A-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2407-2019·2019-09-04
Ad-Tech Medical Recalls Depth Electrodes Due to Incorrect MR Safety Labeling
Ad-Tech Medical Instrument Corporation is recalling depth electrodes because supplemental information incorrectly stated they were approved for use in the MR environment.
Product
Depth Electrodes, Foramen Ovale Depth Electrodes, Macro Micro Depth Electrodes, Spencer Probe Depth Electrodes, Wyler Sphenoidal Depth Electrodes
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2416-2019·2019-09-04
Stryker Endotrac Push Blade Recalled for Compromised Sterile Bag Seal
Stryker GmbH is recalling 251 Endotrac EPF/EGR Push Blades because the sterile bag seal integrity may be compromised.
Product
Endotrac EPF/EGR Push Blade, Catalog Number 3053-1 The EPF system is designed for the treatment of plantar fasciosis. The EPF system is a minimally invasive surgical technique for chronic plantar fasciitis (fasciosis). The EGR system is designed for the treatment of…
Category
Medical Device
Distribution
Distributed nationwide