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.

6551–6575 of 76617

  • ModerateFDA (Devices)·Z-1852-2025·2025-06-04

    Abbott Diagnostics Alinity I Free PSA Reagent Affected by Storage Conditions

    Abbott Diagnostics Alinity I Free PSA reagent units may have been stored outside recommended conditions due to transit delays from severe thunderstorms, potentially affecting test accuracy or timing.

    Product
    ABBOTT DIAGNOSTICS ALINITY I FREE PSA US(200TEST/EA) REAGENT.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1861-2025·2025-06-04

    Straumann Plus Initial Drill missing laser engraving marking

    Straumann USA LLC is recalling Plus Initial Drill units (Article Number 103.170, Lot LNWT8) because the batch was produced without the required 7 mm laser engraving marking.

    Product
    Plus Initial Drill, Article Number: 103.170;
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1822-2025·2025-06-04

    Siemens ADVIA Centaur HCY Calibrator packs recalled for calibrator instability

    Siemens Healthcare Diagnostics is recalling certain lots of ADVIA Centaur HCY Calibrator (2 Pack) due to calibrator instability that causes increased positive bias and fails to meet reference interval specifications in the Instructions for Use.

    Product
    ADVIA Centaur HCY Calibrator (2 Pack). Siemens Material Number: 10310376.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1827-2025·2025-06-04

    HemoCue Glucose 201 Analyzer Microcuvettes Recalled for Storage Conditions

    HemoCue INC F/Glucose 201 Analyzer microcuvettes are being recalled due to transit delays caused by severe thunderstorms that may have resulted in storage outside recommended conditions, which could cause incorrect or delayed test results.

    Product
    HEMOCUE INC F/GLUCOSE 201 ANALYZER (25/VL 4VL/BX) MICROCUVETTE.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1837-2025·2025-06-04

    ORTHO CLINICAL DIAGNOSTICS VITROS BUN Reagent Recall Nationwide

    ORTHO CLINICAL DIAGNOSTICS INC VITROS BUN clinical reagent is being recalled due to transit delays caused by severe thunderstorms that may have exposed products to improper storage conditions, risking incorrect or delayed test results.

    Product
    ORTHO CLINICAL DIAGNOSTICS INC VITROS BUN (60/CR 5CR/PK) ORCLNL REAGENT.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1842-2025·2025-06-04

    Abbott Diagnostics ARCH AUSAB Anti-HBS Reagent Recall

    Abbott Diagnostics ARCH AUSAB Anti-HBS reagent units may have been stored outside recommended temperature conditions due to transit delays caused by severe thunderstorms, potentially leading to incorrect or delayed test results.

    Product
    ABBOTT DIAGNOSTICS ARCH AUSAB ANTI-HBS (100/EA) REAGENT.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1859-2025·2025-06-04

    Ultrasonic Cleaning Systems Triton 36 and 72 recalled

    Ultra Clean Systems, Inc. is recalling Ultrasonic Cleaning Systems Triton 36 and Triton 72 models due to carbon filter sensors breaking down from electrochemical degradation. The defect was identified during routine preventative maintenance checks.

    Product
    Ultrasonic Cleaning Systems Triton 36 Model Number 6003000804 Triton 72 Model Number 6003000805 Ultrasonic cleaning system
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1851-2025·2025-06-04

    Abbott Diagnostics Architect Progesterone Reagent Storage Condition Recall

    Abbott Diagnostics Architect Progesterone (100 tests) reagent is being recalled due to transit delays during severe thunderstorms that may have caused storage outside recommended conditions, risking incorrect or delayed test results.

    Product
    ABBOTT DIAGNOSTICS ARCHITECT PROGESTERONE (100TESTS) REAGENT.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1862-2025·2025-06-04

    GM Helix Acqua Implant labeled 11.5 mm may contain 13 mm

    Straumann USA LLC is recalling GM Helix Acqua Implants (Article Number 140.984) because packages labeled as 11.5 mm implants may contain 13 mm implants instead.

    Product
    GM Helix Acqua Implant, Article Number: 140.984
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1815-2025·2025-06-04

    Apo B Reagent calibration error may produce inaccurate test results

    Beckman Coulter is recalling Apo B Reagent due to an erroneous value in the calibration sheet that could generate incorrect patient test results with positive bias up to 42%.

    Product
    Apo B Reagent, REF: OSR6143
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·019-2025·2025-06-03

    Sulu Organics Recalls Pork Lard and Beef Tallow Lacking Federal Inspection

    Sulu Organics LLC is recalling pork lard and beef tallow products produced without federal inspection. Consumers should not consume these items.

    Product
    Sulu Organics LLC Recalls Pork Lard & Beef Tallow Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V370000·2025-06-03

    2022-2025 Rivian R1T and R1S recalled for unsecured seat belt anchors

    Rivian is recalling certain 2022-2025 R1T and R1S vehicles. D-ring bolts for front seat belt anchorages may not have been properly installed, potentially failing to restrain occupants during a crash.

    Product
    RIVIAN — RIVIAN R1T, R1S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V371000·2025-06-03

    2025 Ford Explorer Brake Caliper Bolts May Be Improperly Secured

    Ford is recalling certain 2025 Explorer vehicles because front brake caliper bolts may not be properly secured, potentially affecting brake function. Dealers will inspect and repair the bolts at no cost.

    Product
    FORD — FORD EXPLORER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-06032025-01·2025-06-03

    USDA Issues Public Health Alert for Organic Ground Beef Due to E. Coli O157:H7

    USDA FSIS issued a public health alert for Organic Rancher ground beef potentially contaminated with E. coli O157:H7. Consumers are urged not to consume the product.

    Product
    NPC Processing, LLC — FSIS Issues Public Health Alert for Ground Beef Products Due to Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·25V373000·2025-06-03

    2025 Hyundai IONIQ 5 Recall: Incorrect Headlight Aim Label

    Hyundai is recalling certain 2025 IONIQ 5 vehicles because the right-side headlight has an incorrect aim label, which can result in improperly aimed headlights that reduce road visibility and increase crash risk.

    Product
    HYUNDAI — HYUNDAI IONIQ 5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·020-2025·2025-06-03

    Springville Meat Recalls Beef Jerky for Undeclared Fish Allergen

    Springville Meat & Cold Storage Co. is recalling beef jerky and snack sticks because they contain undeclared anchovies, a known fish allergen.

    Product
    Springville Meat & Cold Storage Co. Inc. — Springville Meat & Cold Storage Co., Inc., Recalls Beef Jerky/ Beef Snack Stick Products and Voluntarily Inspected Elk, Venison and Buffalo Jerky Products Due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·25V372000·2025-06-03

    2025 Ford Escape Cylinder Head Defect Causes Oil Leaks

    Ford is recalling 2023-2025 Escape and 2025 Bronco Sport vehicles with defective cylinder heads that may cause oil leaks, loss of drive power, and fire risk.

    Product
    FORD — FORD ESCAPE, BRONCO SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V367000·2025-06-02

    Orange EV Recalls 2023-2025 Husk-E Trucks Due to Fire Risk

    Orange EV is recalling 2023-2025 Husk-E terminal trucks because an inadequate fuse in the high-voltage system may fail to open during a short circuit, increasing the risk of fire.

    Product
    ORANGE EV — ORANGE EV HUSK-E
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V342000·2025-06-02

    2024-2025 Battle Motors LET2 Steering Wheel Detachment Recall

    Battle Motors is recalling 2024-2025 LET2 trucks because the steering wheel retaining nut may be improperly tightened, causing the steering wheel to loosen and detach, creating crash risk.

    Product
    BATTLE MOTORS — BATTLE MOTORS LET2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V318000·2025-06-02

    Alliance RV Recalls 2023 Fifth Wheels Due to Freshwater Tank Defect

    Alliance RV is recalling 2023 Paradigm and Avenue fifth wheels because the freshwater tank may be installed incorrectly, posing a road hazard if it detaches.

    Product
    ALLIANCE RV — ALLIANCE RV PARADIGM, AVENUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V369000·2025-06-02

    2023 Mitsubishi Outlander: Rearview Camera Software Defect Recall

    Mitsubishi is recalling 198,940 certain 2022-2024 Outlander and 2023-2025 Outlander PHEV vehicles due to a software error that may freeze or prevent the rearview camera from displaying, reducing rear visibility and increasing crash risk.

    Product
    MITSUBISHI — MITSUBISHI OUTLANDER, OUTLANDER PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V329000·2025-06-02

    Custom Truck Recalls 2020 Ford F-550s Due to Electrical Fire Risk

    Custom Truck is recalling 2020 Ford F-550 vehicles because a firmware defect in Weldon nodes may cause electrical circuits to overheat and increase fire risk.

    Product
    CUSTOM TRUCK & BODY WORKS — CUSTOM TRUCK & BODY WORKS FORD F-550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·25V360000·2025-05-30

    Orange EV Recalls Trucks Due to Steering Shaft Bolt Tightening Issue

    Orange EV is recalling 2022-2025 HUSK-e, e-TRIEVER, and T-Series trucks because improperly tightened steering shaft bolts could cause loss of steering control.

    Product
    ORANGE EV — ORANGE EV HUSK-E, E-TRIEVER, T-SERIES ELECTRIC TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·25V325000·2025-05-30

    Mercedes windshield camera and mirror may be insufficiently attached

    Mercedes-Benz is recalling certain 2024-2025 GLE, GLS and AMG models because the multi-purpose camera and rearview mirror may be insufficiently attached to the windshield and may detach.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH GLE 350 4MATIC, GLE 450E 4MATIC, AMG GLS63 4MATIC+, AMG GLE53 4MATIC+ COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide