The Recall Desk

State

New Mexico product recalls

73,809 recalls have nationwide distribution and so reach New Mexico. 3,638 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total
3,638
Critical
745
Severe
816
Most recent
2026-11-04

Of the 3,638 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 816 (22%) are Severe.

Which agencies issued them

These figures cover only the 3,638 recalls whose distribution notice names New Mexico specifically. The 73,809 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35501–35525 of 77447

  • ModerateFDA (Devices)·Z-1297-2019·2019-05-15

    Elekta Unity Systems Recalled for Missing Contrast Agent Warnings

    Elekta Limited is recalling nine Elekta Unity systems because the user manual lacks a warning regarding the administration of unvalidated contrast agents.

    Product
    Elekta Unity systems Product Usage: Elekta Unity using Magnetic Resonance Imaging is indicated for radiation therapy treatments and stereotactic radiation treatments of malignant and benign diseases anywhere in the body as determined by a licensed medical practitioner in…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1292-2019·2019-05-15

    Ortho-Clinical VITROS ECi/ECiQ Immunodiagnostic System Recalled for Luminometer Malfunction

    Ortho-Clinical Diagnostics is recalling 45 VITROS ECi/ECiQ Immunodiagnostic Systems worldwide due to a luminometer malfunction that may prevent the processing of MicroWell assays.

    Product
    VITROS¿ ECi/ECiQ Immunodiagnostic System Product Code: 1922814 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1290-2019·2019-05-15

    Ortho-Clinical Diagnostics Recalls VITROS 3600 Immunoassay Systems Due to Luminometer Malfunction

    Ortho-Clinical Diagnostics is recalling 28 VITROS 3600 Immunoassay Systems because a luminometer malfunction may prevent the processing of MicroWell assays.

    Product
    VITROS¿ 3600 Immunoassay System Refurbished-Software V3.3.2 & below Product Code: 6802914 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1287-2019·2019-05-15

    Ortho-Clinical Diagnostics Recalls VITROS 5600 Integrated System Software

    Ortho-Clinical Diagnostics is recalling VITROS 5600 Integrated System software versions 3.3.2 and below due to a luminometer malfunction that may prevent the processing of MicroWell assays.

    Product
    VITROS¿ 5600 Integrated System -Software V3.3.2 & below Product Code: 6802413 For use in the in vitro quantitative, semi-quantitative, and qualitative measurement of a variety of analytes of clinical interest, using VITROS Immunodiagnostic Products Reagents
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-1334-2019·2019-05-15

    Schreiber Foods Recalls Colby and Monterey Jack Cheese for Foreign Material

    Schreiber Foods is recalling specific brands of Colby and Monterey Jack cheese due to the presence of hard plastic foreign material.

    Product
    Shredded and blocks of Colby & Monterey Jack cheese - Labeled and Packaged: 1) Great Value, Finely Shredded, Colby & Monterey Jack Cheese, Net Wt 8 oz; packaged in plastic pouches, 12 per case; 2) Great Value, Finely Shredded, Colby & Monterey Jack Cheese, Net Wt 16 oz…
    Category
    Food
    Distribution
    30 states
  • ModerateFDA (Devices)·Z-1301-2019·2019-05-15

    Siemens Atellica Sample Handler Prime Recalled for Software Issues

    Siemens Healthcare Diagnostics is recalling 474 Atellica Sample Handler Prime units due to multiple issues identified in the system software that required an update.

    Product
    Atellica Sample Handler Prime, Material Number 11069001
    Category
    Medical Device
    Distribution
    36 states
  • SevereNHTSA·19V367000·2019-05-14

    Daimler Trucks Recalls 2019 Freightliner and Western Star Trucks for Brake Bolt Issue

    Daimler Trucks North America is recalling 253 specific 2019 heavy-duty trucks because brake caliper mounting bolts may be insufficiently tightened, potentially reducing brake effectiveness.

    Product
    FCCC — FCCC, FREIGHTLINER, WESTERN STAR XCL, XCS, CASCADIA, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V368000·2019-05-14

    2019 Thomas Built Buses Saf-T-Liner C2 Brake Recall

    Daimler Trucks North America is recalling 2019 Thomas Built Buses Saf-T-Liner C2 vehicles because loose brake caliper bolts may reduce braking effectiveness.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER C2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V370000·2019-05-14

    Daimler Trucks Recalls 741 Vehicles for Insufficient Brake Air Reservoir Capacity

    Daimler Trucks North America is recalling 741 Freightliner, Sterling, and Western Star trucks because insufficient air reservoir capacity may reduce brake effectiveness and increase crash risk.

    Product
    STERLING — STERLING, FREIGHTLINER, WESTERN STAR ACTERRA, LT9500, L8500, CLASSIC XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V371000·2019-05-14

    Daimler Trucks Recalls MT55 and MT45 Chassis for Brake Pedal Defect

    Daimler Trucks North America is recalling 2012-2019 Freightliner Custom Chassis MT55 and MT45 vehicles because a brake pedal clip may detach, causing brake light failure or pedal detachment.

    Product
    FCCC — FCCC MT55, MT45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V363000·2019-05-14

    Mazda Recalls 2019 Mazda3 Vehicles for Incorrect Air Bag Indicator Light

    Mazda is recalling 2019 Mazda3 vehicles because the passenger air bag deactivation indicator light may turn off incorrectly, potentially leaving occupants unaware of safety system status.

    Product
    MAZDA — MAZDA MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V364000·2019-05-13

    LDJ Recalls 2019 Thunder Creek Trailers Due to Wheel Lug Nut Issues

    LDJ Manufacturing is recalling 102 2019 Thunder Creek trailers because wheel lug nuts may loosen, potentially causing a wheel to separate and increasing crash risk.

    Product
    THUNDER CREEK — THUNDER CREEK SLT, EV, MTT, FST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V361000·2019-05-13

    Trail King Recalls 2016-2019 TKT50 Trailers Due to Missing Brake Line

    Trail King is recalling 2016-2019 TKT50 trailers because a missing air control line may prevent service brakes from applying on some axles, increasing crash risk.

    Product
    TRAIL KING — TRAIL KING TILT TRAILER (TKT)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V360000·2019-05-13

    Spartan Emergency Chassis Recalled for Brake Valve Defect

    Spartan Motors is recalling 2018-2020 emergency response and motor home chassis because a brake relay valve defect may increase stopping distance.

    Product
    SPARTAN — SPARTAN K3, K2, K4, METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V362000·2019-05-13

    Ford Recalls 2013-2016 Fusion Vehicles for Transmission Shifter Cable Bushing Defect

    Ford is recalling 2013-2016 Fusion vehicles with 2.5-liter engines because a transmission shifter cable bushing may degrade and detach. This could allow the driver to exit the vehicle while the transmission is not in Park, increasing crash risk.

    Product
    FORD — FORD FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V357000·2019-05-13

    Lance Camper Recalls 2019-2020 Truck Campers Due to Bunk Bed Gap

    Lance Camper is recalling 2019-2020 855S and 1172 Truck Campers because a gap in the fold-down bunk bed may allow occupants to fall and get stuck.

    Product
    LANCE CAMPER — LANCE CAMPER TRUCK CAMPER (855S), TRUCK CAMPER (1172)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V359000·2019-05-13

    Unruh Fire Recalls One 2018 RAM 5500 Fire Truck for Brake Light Defect

    Unruh Fire is recalling one 2018 RAM 5500-based fire truck because its brake lights may illuminate without the brake pedal being pressed, potentially confusing other drivers.

    Product
    RAM — RAM 5500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V356000·2019-05-10

    Forest River Recalls 2019-2020 R-POD Travel Trailers Due to Fire Risk

    Forest River is recalling 2019-2020 R-POD travel trailers because a refrigerator wire may be connected to a breaker that allows too much current, increasing the risk of fire.

    Product
    FOREST RIVER — FOREST RIVER R-POD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V355000·2019-05-10

    Forest River Cherokee Travel Trailer Recall for Incorrect Federal Placard

    Forest River is recalling 2018-2019 Cherokee travel trailers because the Federal Placard may list incorrect axle and capacity information, potentially leading to vehicle overload.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide