State

New Mexico product recalls

73,092 recalls have nationwide distribution and so reach New Mexico. 3,628 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total: 3,628
Critical: 747
Severe: 649
Most recent: 2026-09-23

Of the 3,628 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 649 (18%) are Severe.

Which agencies issued them

These figures cover only the 3,628 recalls whose distribution notice names New Mexico specifically. The 73,092 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

7601–7625 of 76720

CriticalFDA (Devices)·Z-1244-2025·2025-03-12
Rotarex Atherectomy Catheter Recalled for Helix Fracture Risk
Bard is recalling Rotarex Atherectomy System catheters due to potential helix fracture or breakage that could cause vessel injury and severe bleeding. Updated instructions are being distributed to clarify procedural steps to reduce this risk.
Product
Rotarex Atherectomy System and Instructions for Use, BD SET Rotarex: S 6 F x 110 cm, REF: 80236; S 6 F x 135 cm, REF: 80237; S 8 F x 85 cm, REF: 80238; S 8 F x 110 cm, REF: 80239
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V152000·2025-03-12
Shyft Recalls 2025 Utilimaster Upfit Vehicles for Loose Seat Bolts
Shyft Group is recalling 2025 Utilimaster Upfit vehicles because passenger jump seat mounting bolts may not be properly tightened, increasing injury risk in a crash.
Product
UTILIMASTER — UTILIMASTER UPFIT
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·25V154000·2025-03-12
BMW X3 rear brake hoses may leak and disable rear braking
BMW is recalling certain 2025 X3 30 xDrive and X3 M50 xDrive vehicles because the rear brake hoses may leak, causing a loss of rear brake function, ABS and stability control.
Product
BMW — BMW X3
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1245-2025·2025-03-12
Medtronic Pipeline Vantage Embolization Device Recall for Structural Deformation Risk
Medtronic is recalling approximately 18,245 unused Pipeline Vantage embolization devices due to incomplete wall apposition and braid deformation that may lead to thrombosis and serious adverse events.
Product
Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-027-350-12, PED3-027-350-14, PED3-027-350-16, PED3-027-350-20, PED3-027-350-25, PED3-027-400-12, PED3-027-400-14, PED3-027-400-16, PED3-027-400-18, PED3-027-400-20, PED3-027-400-25, PED3-027-400-30,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1263-2025·2025-03-12
Insulin Pump Recalled for Abnormal Delivery During Flight Pressure Changes
Medtronic MiniMed 720G insulin pumps may malfunction during airplane travel due to air pressure changes, causing abnormal insulin doses that can lead to severe low or high blood sugar emergencies.
Product
MiniMed insulin pump, REF: 720G (MMT-1809, MMT-1810, MMT-1859, MMT-1860, MMT-1867)
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·25V046000·2025-03-12
Freightliner Recalls eCascadia and eM2 Trucks for Power Loss Risk
Daimler Trucks North America is recalling 2020-2026 Freightliner eCascadia and eM2 trucks because a faulty power module may cause a loss of drive power, increasing crash risk.
Product
FREIGHTLINER — FREIGHTLINER EM2, E-CASCADIA
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1254-2025·2025-03-12
Baxter Spectrum IQ Infusion System may have missing motor mounting screws
Baxter Spectrum IQ Infusion Systems may lack motor mounting screws due to a servicing defect. The FDA Class I recall affects 323 units distributed nationwide.
Product
Baxter Spectrum IQ Infusion System with Dose IQ Safety Software, Product Code 3570009
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1246-2025·2025-03-12
Medtronic Pipeline Vantage device recall: deformation may cause blood clots
The Pipeline Vantage Embolization Device may malfunction, with the braid deforming or not positioning correctly, potentially causing blood clots. Approximately 7,820 units are affected worldwide.
Product
Medtronic Pipeline Vantage Embolization Device with Shield Technology, REF: PED3-021-350-16, PED3-021-250-14, PED3-021-350-20, PED3-021-250-20, PED3-021-300-16, PED3-021-300-20, PED3-021-275-12, PED3-021-275-16, PED3-021-325-12, PED3-021-325-14, PED3-021-325-16, PED3-021-325-20,
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Food)·F-0607-2025·2025-03-12
Frozen Sugar Cookie Dough Recalled for Undeclared Egg Allergen
Amazon Fresh Bake at Home Jumbo Sugar Cookie dough is being recalled due to undeclared egg. Consumers with egg allergies should not consume this product.
Product
ASIN B0CY2RDW5T, Amazon Fresh brand, Bake at Home Jumbo Sugar Cookie 30oz, product is frozen dough, and packaged in flexible plastic bag. UPC 446472006995.
Category
Food
Distribution
Distributed nationwide
SevereFDA (Food)·F-0606-2025·2025-03-12
Amazon Fresh Jumbo Sugar Cookies recalled for undeclared egg allergen
Amazon Retail LLC is recalling Amazon Fresh Jumbo Sugar Cookies nationwide due to undeclared egg, a major allergen. Consumers with egg allergies should not consume the affected cookies.
Product
ASIN B084PZ7K98, Amazon Fresh Jumbo Sugar Cookie, 27 oz (12 count), product is baked and packaged in flexible plastic bag. 4-day shelf life. UPC 465712007998. ASIN B084PX9V31, Amazon Fresh Jumbo Sugar Cookie, 2.3 oz (1 count), product is baked and sold from open pastry tray in s
Category
Food
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1253-2025·2025-03-12
Baxter Sigma Spectrum Infusion System Recalled for Missing Mounting Screws
Baxter Healthcare is recalling 66 units of Sigma Spectrum Infusion System (V6) due to potential missing motor mounting screws that may have occurred during servicing. Missing screws could affect the device's operation.
Product
Baxter Sigma Spectrum Infusion System (V6 Platform), Product Code 35700BAX
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1255-2025·2025-03-12
Medtronic Paradigm insulin pumps may deliver incorrect doses during flight
Medtronic MiniMed insulin pumps may deliver abnormally high or low insulin doses in response to air pressure changes during airplane takeoff and landing, potentially causing severe hypoglycemia or hyperglycemia.
Product
Paradigm REF: MMT-712 and MMT-715
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1260-2025·2025-03-12
Medtronic MiniMed Insulin Pumps Recalled for Abnormal Delivery During Air Pressure Changes
Medtronic is recalling MiniMed insulin pumps that malfunction during airplane takeoff and landing due to air pressure changes. The defect can cause abnormal insulin delivery, leading to severe hypoglycemia, hyperglycemia, seizure, coma, or death.
Product
MiniMed insulin pump, REF: 640G (MMT-1711, MMT-1712, MMT-1751, MMT-1752)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0256-2025·2025-03-12
Nelarabine prescription injection recalled due to failed quality specifications
Zydus Pharmaceuticals is recalling 1,893 vials of Nelarabine Injection (250 mg/50 mL) due to failed quality specifications for impurities and degradation. Patients should contact their healthcare provider about the recall.
Product
NELARABINE — NELARABINE (NELARABINE)
Category
Drug
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1294-2025·2025-03-12
Tissue Approximation System zip-ties at risk of breaking during implantation
TAS Medical is recalling Tissue Approximation System models because tissue approximation straps (zip-ties) may break before or during surgery. Undetected breaks could lead to hernia recurrence requiring additional corrective surgery.
Product
TISSUE APPROXIMATION SYSTEM (TAS), Models T-4000, T-5000, T-LAP
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1270-2025·2025-03-12
Philips BGM 4 Blood Glucose Meter Battery Expansion Risk Recall
Telcare recalls 34,764 Philips BGM 4 blood glucose meters (Model TM0009) nationwide due to battery expansion and swelling. The battery may cause the back cover to separate or, in worst-case scenarios, explode. No injuries reported to date.
Product
Philips Connected Blood Glucose Meter, BGM 4; Model Number: TM0009;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1250-2025·2025-03-12
TBS iNsight bone density software calculation variability on Hologic machines
TBS iNsight medical device software may produce inconsistent calculation results when operating on Hologic Horizon bone densitometers, particularly when comparing fast array scans to standard array scans.
Product
Brand Name: TBS Osteo Product Name: TBS iNsight Model/Catalog Number: TBS iNsight v3.x / pn: OS-TBSi Software Version: V3.x: (1) V3.1.2, (2) V3.1.1, (3) V3.1.0, (4)V3.0.0 Product Description: TBS iNsight is a class II Medical Device software that is installed on bone densitom
Category
Medical Device
Distribution
23 states
HighFDA (Devices)·Z-1261-2025·2025-03-12
Medtronic MiniMed insulin pump recalled for air pressure-triggered delivery defect
Medtronic MiniMed insulin pumps can deliver abnormal insulin doses during air pressure changes in airplane travel, risking severe hypoglycemia or hyperglycemia and serious complications.
Product
MiniMed insulin pump, REF: 670G (MMT-1760, MMT-1761, MMT-1762, MMT-1780, MMT-1781, MMT-1782)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1276-2025·2025-03-12
Osstem dental implant abutments mislabeled on patient chart stickers
Hiossen is recalling 119 Osstem dental implant abutments because patient chart stickers incorrectly identify product versions. ET Rigid and ET Multi abutments are labeled backwards, potentially leading to selection of the wrong abutment size.
Product
Osstem Implant System - Abutment: ET Multi AbutmentSize: 4.8D 5.0GH - Abutment is intended for use with a dental implant to provide suport for prosthetic restorations such as crowns, bridges, or overdentures. Model/Catalog Number: ETMTA505RV1
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1265-2025·2025-03-12
MiniMed Insulin Pump May Malfunction at High Altitude During Flight
Medtronic MiniMed insulin pumps may deliver abnormal insulin doses during airplane takeoff or landing due to air pressure changes, potentially causing severe low or high blood sugar.
Product
MiniMed insulin pump, REF: 770G (MMT-1880, MMT-1881, MMT-1882, MMT-1890, MMT-1891, MMT-1892)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1267-2025·2025-03-12
MIM Radiological Imaging Software Versions May Generate Incorrect Diagnostic Values
MIM radiological software versions 7.2.0-7.2.6 may produce incorrect readings when fusing images with different fields of view, which could affect diagnostic accuracy.
Product
MIM software; System, Image Processing, Radiological
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·25V155000·2025-03-12
Land Rover Recalls 2025 Range Rovers for Seat Belt Defect
Jaguar Land Rover is recalling 2025 Range Rover and Range Rover Sport vehicles because the second-row center seat belt buckle may not latch correctly.
Product
LAND ROVER — LAND ROVER RANGE ROVER, RANGE ROVER SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·25C004000·2025-03-12
Dorel Recalls Safety 1st Child Seats Due to Incorrect Height Labeling
Dorel Juvenile Group is recalling specific Safety 1st 3-in-1 child seats because the forward-facing installation label incorrectly states the height range, which may lead to improper restraint.
Product
CHILD SEAT recall
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1259-2025·2025-03-12
MiniMed Insulin Pumps Recalled for Abnormal Insulin Delivery During Flight
MiniMed insulin pumps may deliver abnormal insulin doses during aircraft takeoff and landing due to air pressure changes, risking severe blood sugar fluctuations, seizures, and potentially fatal complications.
Product
MiniMed insulin pump, REF: 630G (MMT-1714, MMT-1715, MMT-1754, MMT-1755)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0253-2025·2025-03-12
Lorazepam Oral Syringes Recalled Due to Defective Delivery System Causing Leakage
Safecor Health, LLC is recalling Lorazepam 0.5 mg oral syringes nationwide due to a defective delivery system that causes leakage after repackaging.
Product
Lorazepam 0.5 mg per 0.25 mL Oral Syringe, Delivers: 0.25 mL, Oral Concentrate, Rx Only, Refrigerate, Mfg by: PAI, Pkg by: Safecor Health, LLC, Columbus, OH 43204, NDC: a) 00054353244, b) 00121077001, c) 65162068784.
Category
Drug
Distribution
Distributed nationwide