The Recall Desk

State

New Mexico product recalls

73,737 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.

These figures cover only the 3,636 recalls whose distribution notice names New Mexico specifically. The 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29751–29775 of 77373

  • SevereNHTSA·20V365000·2020-06-23

    Ford Recalls 2020 Super-Duty Pickups for Transmission Defect

    Ford is recalling 2020 F-250, F-350, and F-550 Super-Duty diesel pickups because a brittle transmission part may fracture, causing engine stalls or increased braking effort.

    Product
    FORD — FORD F-250 SD, F-550 SD, F-350 SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V367000·2020-06-23

    Newell P50 Motor Coaches Recalled for Brake Pedal Obstruction Risk

    Newell is recalling 2020-2021 P50 motor coaches because a decorative cover may become lodged under the brake pedal, potentially impacting the ability to stop.

    Product
    NEWELL — NEWELL P50
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V366000·2020-06-23

    Ford Recalls 2020 Expedition and Lincoln Navigator for Headrest Weld Defect

    Ford is recalling 2020 Expedition and Lincoln Navigator vehicles because a driver's side second-row seat headrest bracket may be improperly welded, potentially failing to restrain occupants in a crash.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V364000·2020-06-22

    Mercedes-Benz Recalls 2020 Models for Turbocharger Oil Leak Fire Risk

    Mercedes-Benz is recalling 2020 C300, E350, and GLC300 vehicles because improperly tightened turbocharger oil line screws may cause leaks that increase fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 350, C 300, GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalNHTSA·20V360000·2020-06-19

    Forest River Surveyor Recalled for Furnace Carbon Monoxide Risk

    Forest River is recalling 2020 Surveyor trailers because a furnace may detach from the exhaust vent, creating a carbon monoxide hazard.

    Product
    FOREST RIVER — FOREST RIVER SURVEYOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V361000·2020-06-19

    2021 Forest River FR3 Leveling Jack Wiring Defect Poses Crash Risk

    The 2021 Forest River FR3 recreational vehicle has a wiring harness defect that can cause leveling jacks to deploy while driving, risking loss of vehicle control. Forest River will provide free repairs.

    Product
    FOREST RIVER — FOREST RIVER FR3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V363000·2020-06-19

    2020-2021 Motorhomes Recalled for Brake Hose Chafing Risk

    Certain 2020-2021 motorhomes built on Sprinter chassis may develop a brake hose chafed by the fender liner, potentially losing brake fluid. Owners should have dealers inspect and replace brake hoses and modify fender liners at no cost.

    Product
    COACHMEN — COACHMEN, DYNAMAX, FOREST RIVER GALLERIA, ISATA, BATTISTI, SUNSEEKER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V362000·2020-06-19

    Grand Design Recalls 2016-2018 Reflection Trailers for Wiring Fire Risk

    Grand Design is recalling 2016-2018 Reflection trailers because a wiring connector may allow water intrusion, potentially causing an electrical short circuit and fire.

    Product
    GRAND DESIGN — GRAND DESIGN REFLECTION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·20141·2020-06-18

    Lochinvar Recalls Residential Boilers Due to Carbon Monoxide Risk

    Lochinvar is recalling about 34,300 residential boilers because a flue grommet can fail, allowing carbon monoxide to escape. Consumers should contact a technician for a free repair.

    Product
    Lochinvar condensing residential boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·20752·2020-06-18

    Modus Furniture Recalls Dressers Due to Tip-Over and Entrapment Hazards

    Modus Furniture is recalling Brighton, Travis, and Bevelle dressers because they are unstable without mirrors, posing tip-over and entrapment risks to children.

    Product
    Brighton, Travis and Bevelle dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2349-2020·2020-06-17

    RayStation 9A Software Recall for Dose Calculation Errors

    RaySearch Laboratories is recalling RayStation 9A software due to errors in dose calculation algorithms that could underestimate radiation therapy doses.

    Product
    RayStation 9A, UDI # 07350002010174 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2263-2020·2020-06-17

    Endologix Ovation iX Abdominal Stent Graft Systems Recalled for Polymer Leak Risk

    Endologix is recalling Ovation iX Abdominal Stent Graft Systems because a material weakness may cause polymer leaks during implantation, potentially leading to clinical events.

    Product
    Ovation iX Abdominal Stent Graft Systems, REF: TV-AB2080-I, TV-AB2080-J, TV-AB2380-I, TV-AB2380-J, TV-AB2680-I, TV-AB2680-J, TV-AB2980-I, TV-AB2980-J, TV-AB3480-I, TV-AB3480-J
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·20138·2020-06-17

    Rexair Recalls Rainbow SRX Vacuums Due to Fire and Burn Hazards

    Rexair is recalling about 38,000 Rainbow SRX vacuums because the circuit board can spark, posing fire and burn hazards. Two fires have been reported.

    Product
    Rainbow SRX Vacuums
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2348-2020·2020-06-17

    RayStation 8B Software Recall for Dose Calculation Errors

    RaySearch Laboratories is recalling RayStation 8B Service Pack 2 software due to a defect in dose calculation algorithms that could underestimate radiation dose.

    Product
    RayStation 8B Service Pack 2, UDI # 07350002010235 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2340-2020·2020-06-17

    RayStation 5 Service Pack 3 Radiation Therapy Software Recalled

    RaySearch Laboratories is recalling RayStation 5 Service Pack 3 software due to a dose calculation error that may underestimate radiation dose.

    Product
    RayStation 5 Service Pack 3, UDI # 07350002010020 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2326-2020·2020-06-17

    Canon Medical System Recalls 24 Infinix-8000C Digital Radiography Systems

    Canon Medical System is recalling 24 Infinix-8000C digital radiography systems because loose bolts may cause the catheterization table to tilt.

    Product
    Infinix-8000C with Catheterization Table CAT-850B or CAT-860B - Product Usage: This device is a digital radiography/fluoroscopy system used in a diagnostic and interventional angiography configuration. The system is indicated for use in diagnostic and angiographic procedures for…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-2342-2020·2020-06-17

    RayStation 6 Service Pack 2 Radiation Therapy Software Recalled for Dose Calculation Error

    RaySearch Laboratories is recalling RayStation 6 Service Pack 2 software due to a calculation error that could underestimate radiation dose.

    Product
    RayStation 6 Service Pack 2, UDI # 07350002010075 - Product Usage: For radiation therapy and medical oncology which can also be used to administer treatments.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1302-2020·2020-06-17

    QuVa Pharma Recalls Subpotent Oxytocin Injection Bags

    QuVa Pharma is recalling 648 bags of oxyTOCIN 30 Units/500 mL because the product did not contain the active drug.

    Product
    oxyTOCIN 30 Units/500 mL (0.06 Units/mL) added to 0.9% Sodium Chloride Injection for IV Use, Rx only, QuVa Pharma 1075 West Park One Drive, Suite 100 Sugar Land, TX 77478 888-339-0874, NDC 70092-1068-07
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V359000·2020-06-17

    Volkswagen Recalls 2020 Jetta for Loose Front Brake Caliper Bolts

    Volkswagen is recalling one 2020 Jetta because front brake caliper bolts may come loose, potentially affecting brake performance and increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2305-2020·2020-06-17

    Biomet A.L.P.S. Proximal Humerus Plating System Drill Block Set Screw Recalled

    Biomet is recalling A.L.P.S. Proximal Humerus Plating System Drill Block Set Screws because they were distributed without completed design history files or design transfer activities.

    Product
    A.L.P.S. PROXIMAL HUMERUS PLATING SYSTEM DRILL BLOCK SET SCREW, Item Number: 110017551 - Product Usage: Intended for temporary internal fixation and stabilization of osteotomies and fractures during the normal healing process.
    Category
    Medical Device
    Distribution
    Distributed nationwide