The Recall Desk

State

New Mexico product recalls

72,992 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.

These figures cover only the 3,625 recalls whose distribution notice names New Mexico specifically. The 72,992 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

6251–6275 of 76617

  • ModerateFDA (Drugs)·D-0489-2025·2025-07-02

    Dobutamine Injection Recall Due to Discoloration and Cracked Vials

    Pfizer is recalling one lot of Dobutamine Injection (250 mg/20 mL) nationwide due to discoloration and discolored solution caused by cracked vials. Healthcare facilities should quarantine and return affected units.

    Product
    DOBUTAMINE — DOBUTAMINE (DOBUTAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·H-0091-2025·2025-07-02

    Prothin Dietary Supplement Recall for Undeclared Food Dyes

    Preventics, Inc. is recalling Prothin dietary supplement packets because they contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) in the gelatin capsules, which may affect consumers with dye sensitivities or allergies.

    Product
    Prothin, dietary supplement. Seven Packets containing 2 tablets and 4 capsules. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2026-2025·2025-07-02

    Jewel Precision Reusable Rigid Sterilization Container System Instructions Mismatch

    Jewel Precision Reusable Rigid Sterilization Container System (Model JP-24-6) is being recalled because the Instructions for Use do not match the FDA-cleared indications for use or sterility shelf life.

    Product
    Jewel Precision Reusable Rigid Sterilization Container System. Model/Catalog Number: JP-24-6.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2027-2025·2025-07-02

    Atellica CH Diluent Contaminated with Sodium Hypochlorite

    Siemens Healthcare Diagnostics is recalling Atellica CH Diluent (SMN 11099300, Lot 0000195412) due to contamination with sodium hypochlorite, which may affect laboratory test results.

    Product
    Product: Atellica CH Diluent - CONS 2 x 1.5L; Siemens Material Number (SMN): 11099300;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0483-2025·2025-07-02

    Tirzepatide Injections Pre-filled Syringe Recalled for Sterility Assurance

    Thrive Health Solutions is recalling Tirzepatide Injections 20mg/mL pre-filled syringes due to lack of assurance of sterility. Approximately 826 syringes distributed nationwide are affected.

    Product
    Tirzepatide Injections, 20mg/mL, pre-filled syringe, Thrive Health Solutions, 88 Inverness, Cir E, Suite A-204, Englewood, CO 80112
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0095-2025·2025-07-02

    NutriLean Dietary Supplement Contains Undeclared Food Dyes

    Preventics, Inc. dba Legere Pharmaceuticals is recalling NutriLean dietary supplements nationwide because the gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1) food dyes, which are not listed on the label.

    Product
    NutriLean, dietary supplement. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Food)·H-0096-2025·2025-07-02

    Rodex Forte dietary supplement recalled for undeclared food dyes

    Rodex Forte dietary supplement (90-capsule bottles) is being recalled because the gelatin capsules contain undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No. 1), which are not listed on the label.

    Product
    Rodex Forte, dietary supplement. 90 capsule bottles. Legere Pharmaceuticals 15344 N 83rd way, Scottsdale AZ 85260 (Product does not have a UPC)
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V434000·2025-06-30

    Volkswagen chassis, brake and suspension bolts may be incorrectly tightened

    Volkswagen is recalling certain 2023-2025 Atlas, Atlas Cross Sport and 2023-2024 ID.4 vehicles because bolts on the chassis, brake system and suspension may not have been correctly tightened in manufacturing.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS CROSS SPORT, ID.4, ATLAS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V428000·2025-06-27

    Audi Recalls 2025 E-Tron GT Vehicles Due to Suspension Strut Defect

    Volkswagen Group of America is recalling 2025 Audi E-Tron GT vehicles because a retaining ring on the front suspension strut may come loose, potentially causing air loss and loss of vehicle control.

    Product
    AUDI — AUDI E-TRON GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V431000·2025-06-27

    Newmar motorhome baggage door skins can separate from the door frame

    Newmar is recalling certain 2016-2024 King Aire, 2023-2024 London Aire and Essex motorhomes because the baggage door skins may come loose and separate from the door frame.

    Product
    NEWMAR — NEWMAR ESSEX, KING AIRE, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V440000·2025-06-27

    Freightliner Recalls 2026 Cascadia Fifth Gen Trucks for Fuel Line Routing Defect

    Daimler Trucks North America is recalling 2026 Freightliner Cascadia Fifth Gen trucks because an incorrectly routed fuel line can damage brake lines and wiring, increasing crash and fire risks.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA FIFTH GEN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V438000·2025-06-27

    Ford Recalls 2025 F-150 Lightning BEV Due to Brake Hose Bracket Issue

    Ford is recalling 2025 F-150 Lightning BEV vehicles because front brake jounce hose bracket screws may loosen, causing a brake fluid leak that increases stopping distance.

    Product
    FORD — FORD F-150 LIGHTNING BEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V443000·2025-06-27

    Ford Recalls 2017 GT Models for Rear Wing Hydraulic Leak Risk

    Ford is recalling 2017 GT vehicles previously repaired under recall 18V707 because the rear wing valve block may leak hydraulic fluid, increasing fire risk.

    Product
    FORD — FORD GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V445000·2025-06-27

    Orange EV Recalls HUSK-E Trucks for Electrical Fire Risk

    Orange EV is recalling 2023-2025 HUSK-E terminal trucks because an incorrect washer size installed during a previous repair can cause electrical arcing and increase the risk of fire.

    Product
    ORANGE EV — ORANGE EV HUSK-E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V437000·2025-06-27

    Nissan and Infiniti VC-Turbo engine bearings may cause engine failure

    Nissan is recalling certain 2019-2024 Rogue, Altima, Infiniti QX50 and QX55 vehicles with VC-Turbo engines because engine bearing defects can lead to engine failure and, if the block is breached, an engine fire.

    Product
    INFINITI — INFINITI, NISSAN QX50, ROGUE, QX55, ALTIMA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V439000·2025-06-27

    Ford Expedition and Navigator passenger airbags may deploy with excessive force

    Ford is recalling certain 2025 Navigator and Expedition vehicles because the passenger side airbag may have been manufactured incorrectly and can deploy with excessive force during a crash.

    Product
    FORD — FORD, LINCOLN EXPEDITION, NAVIGATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V441000·2025-06-27

    Ford Recalls 2022 Mustang Mach E Vehicles for Battery Contactor Overheating

    Ford is recalling 2022 Mustang Mach E vehicles with extended range batteries because high voltage contactors may overheat, potentially causing loss of drive power and increasing crash risk.

    Product
    FORD — FORD MUSTANG MACH E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V444000·2025-06-27

    Oshkosh Recalls 2025 NGDV Vehicles for Detaching Air Bag Warning Label

    Oshkosh is recalling 2025 NGDV and NGDV Electric vehicles because the air bag warning label on the sun visor may detach, failing federal safety standards.

    Product
    OSHKOSH — OSHKOSH NGDV, NGDV ELECTRIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V442000·2025-06-27

    Ford rearview cameras may show a blank or persistent image

    Ford is recalling a wide range of 2018-2024 vehicles because a software error may cause the rearview camera to display a blank image, or leave the image on screen after backing has ended.

    Product
    FORD — FORD, LINCOLN F-250 SD, ECOSPORT, EDGE, FUSION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·25V417000·2025-06-27

    Bowlus trailer manual omits hitch bolt retightening from maintenance schedule

    Bowlus is recalling certain trailers with an elongated hitch because the owner's manual does not include instructions to retighten the two hitch bolts in the maintenance schedule.

    Product
    BOWLUS — BOWLUS ENDLESS HIGHWAYS, TERRA FIRMA, VOLTERRA, RIVET
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • LowUSDA FSIS·024-2025·2025-06-27

    Gaiser's Recalls Ready-to-Eat Bologna Due to Undeclared Meat Ingredients

    Gaiser's European Style Provisions is recalling approximately 143,416 pounds of ready-to-eat bologna products because they contain undeclared meat or poultry ingredients.

    Product
    Gaiser's European Style Provisions Inc. — Gaiser's European Style Provisions Inc. Recalls Ready-To-Eat Meat and Poultry Bologna Products Due to Misbranding
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereCPSC·25362·2025-06-26

    Vevor Single Post Handrails Recalled Due to Welding Failure Injury Hazard

    Sanven Technology (Vevor) is recalling about 360 single post handrails for one or two step stairs because the welding can break while in use, posing an injury hazard. Five incidents of handrails breaking have been reported, including one head injury.

    Product
    Vevor Single Post Handrails
    Category
    Consumer Product
    Distribution
    Distributed nationwide