The Recall Desk

State

New Mexico product recalls

73,509 recalls have nationwide distribution and so reach New Mexico. 3,629 additional recalls listed New Mexico specifically in their distribution scope.

What the numbers show

Total
3,629
Critical
747
Severe
813
Most recent
2026-10-14

Of the 3,629 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 813 (22%) are Severe.

Which agencies issued them

These figures cover only the 3,629 recalls whose distribution notice names New Mexico specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22476–22500 of 77138

  • ModerateFDA (Drugs)·D-0635-2022·2022-03-09

    70% Isopropyl Alcohol First Aid Antiseptic Contains Undeclared Ethyl Alcohol

    TSM Brands LLC is recalling 70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen due to undeclared ethyl alcohol in the product. The recall affects bottles distributed nationwide.

    Product
    70% Isopropyl Alcohol First Aid Antiseptic with Wintergreen, 12 FL. OZ. 355 ML bottle, Distributed By: TSM Brands LLC, 540 Equinox LN, Manalapan, NJ 07726, www.tsmbrands.com, Made in Turkey, UPC 868275965765
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0697-2022·2022-03-09

    Microbiologics QC Panel Recalled Due to Shelf Life Testing Failure

    Microbiologics Inc is recalling its Helix Elite Extended Enteric Bacterial Verification Panel because real-time shelf life testing failed at 24 months.

    Product
    Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial Verification Panel (Inactivated Pellet) includes 21 pellets each comprised of the following 8 organisms: 1. S. Typhimurium derived from NCTC 74, 2. S. sonnei derived from NCTC 12984, 3. E. coli…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0632-2022·2022-03-09

    Amlodipine and Olmesartan Medoxomil Tablets Recalled for cGMP Deviations

    Macleods Pharma USA is recalling one lot of Amlodipine and Olmesartan Medoxomil Tablets nationwide due to current Good Manufacturing Practice (cGMP) deviations. The recall is voluntary and was initiated by the manufacturer.

    Product
    AMLODIPINE AND OLMESARTAN MEDOXOMIL — AMLODIPINE AND OLMESARTAN MEDOXOMIL (AMLODIPINE AND OLMESARTAN MEDOXOMIL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0703-2022·2022-03-09

    QC Control Sets for GBS Testing Recalled Due to Contamination

    Microbiologics QC sets used for GBS testing contain a negative control contaminated with Group B Streptococcus, causing test failures. Affects 541 units distributed nationwide.

    Product
    QC Sets and Panels: KWIK-STIK. Cepheid Xpert GBS QC Set (Live Culture). Sets include: 1. 0864E3 Streptococcus agalactiae (Group B, lb) derived from ATCC 12401; 2. 0864E5 Streptococcus agalactiae (Group B, lb) derived from ATCC 12401; 3. 0864E7 Streptococcus agalactiae…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0642-2022·2022-03-09

    Alprazolam Tablets 1mg Recalled for CGMP Deviations

    Preferred Pharmaceuticals is recalling 276 bottles of Alprazolam Tablets USP 1mg (generic Xanax) distributed nationwide due to Current Good Manufacturing Practice (CGMP) deviations. The recall was initiated voluntarily by the manufacturer.

    Product
    Alprazolam Tablets, USP 1mg, Generic for Xanax, Pkg Size: a) 30 tablets per bottle, NDC: 68788-6381-03, b) 60 tablets per bottle, NDC: 68788-6381-06, c) 90 tablets per bottle, NDC: 68788-6381-09, Mfg: Par Pharmaceutical.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0713-2022·2022-03-09

    LYFO-DISK Quality Control Kit Lot Fails Antibiotic Resistance Specification

    A lot of LYFO-DISK quality control kit was found susceptible to Gentamicin Synergy when it should have been resistant. The 153 affected units were distributed worldwide.

    Product
    LYFO-DISK, Quality control kit for culture media, sold as: LYFO-DISK Enterococcus faecalis derived from ATCC 51299
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0683-2022·2022-03-09

    BioPro Titanium MPJ Toe Implant Recalled for Incorrect MR Compatibility Labeling

    BioPro is recalling Titanium MPJ toe implants because instructions and patient cards falsely claim the devices are compatible with MRI imaging, when safety testing for this titanium version has not been conducted.

    Product
    Titanium MPJ (Toe Implant) TOE JOINT TITANIUM NPC MD, Part ID 16814
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0639-2022·2022-03-09

    Olanzapine 10 mg tablets recalled due to cGMP deviations

    Macleods Pharma USA is voluntarily recalling Olanzapine 10 mg tablets nationwide due to cGMP (current good manufacturing practices) deviations identified during manufacturing. The recall affects 3,672 bottles distributed across the United States.

    Product
    OLANZAPINE — OLANZAPINE (OLANZAPINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0713-2022·2022-03-09

    Dexamethasone Elixir Recalled for Impurities Above Permissible Levels

    Morton Grove Pharmaceuticals is recalling Dexamethasone Elixir USP 0.5 mg/5 mL nationwide due to unknown impurities found at higher than permissible levels in affected lots.

    Product
    Dexamethasone Elixir, USP 0.5 mg/5 mL, Net: 8 fl oz (237 mL) bottle, Rx only, Manufactured By: Morton Grove Pharmaceuticals, Inc., Morton Grove, IL 60053, NDC 60432-466-08.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V136000·2022-03-08

    Triple E Recalls Motorhomes Due to Missing Refrigerator Exhaust Deflectors

    Triple E is recalling 2010-2014 Unity, Libero, and Serenity motorhomes because missing refrigerator exhaust deflectors allow heat to overheat the wood frame, posing a fire risk.

    Product
    TRIPLE E — TRIPLE E SERENITY, LIBERO, UNITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V131000·2022-03-08

    Mercedes-Benz Recalls 2021 Sprinter Vans Due to Torsion Bar Assembly Error

    Daimler Vans USA is recalling 2,153 2021 Mercedes-Benz Sprinter vans because an incorrectly installed shim on the torsion bar may fail, causing loss of vehicle stability and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 4500, SPRINTER 3500, SPRINTER 2500, SPRINTER 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V134000·2022-03-08

    Mercedes-Benz Recalls Metris Vans Due to Fuel Hose Leak Risk

    Daimler Vans USA is recalling 2017-2022 Mercedes-Benz Metris vehicles because insecure fuel hose connections may cause leaks, increasing fire risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V138000·2022-03-08

    Terex Recalls 2016-2021 Aerial Devices Due to Emergency Stop Defect

    Terex is recalling 2016-2021 OM, Optima-HRX, and TCX aerial devices because emergency stop controls may fail to stop all boom functions, increasing injury risk.

    Product
    TEREX — TEREX OPTIMA TCX, OPTIMA HRX, OM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V135000·2022-03-08

    2022 Forest River Cardinal travel trailers recalled for electrical fire risk

    Forest River is recalling certain 2022 Cardinal and related travel trailers due to a loose wire cord at the 50AMP shore power inlet that may cause an electrical short and fire.

    Product
    COACHMEN — COACHMEN, FOREST RIVER FREEDOM EXPRESS, CHEROKEE, SABRE, APEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V130000·2022-03-07

    Yamaha Recalls 2021-2022 MT-09 and Tracer 9 GT Motorcycles for ECU Defect

    Yamaha is recalling 2021-2022 MT-09 and Tracer 9 GT motorcycles because improper ECU programming may cause engine stalls or limit throttle response, increasing crash risk.

    Product
    YAMAHA — YAMAHA MT-09, TRACER 9, TRACER 9 GT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V132000·2022-03-07

    Ubco Recalls 2021-2022 2X2 ADV Motorcycles Due to Wheel Hub Gear Defect

    Ubco is recalling 2021-2022 2X2 ADV motorcycles because a wheel hub gear may loosen and contact the motor, potentially causing the wheel to seize and increasing crash risk.

    Product
    UBCO — UBCO 2X2 ADV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V125000·2022-03-04

    Mercedes-Benz Recalls 2020-2021 Models for Rear Brake Caliper Fastener Issue

    Mercedes-Benz is recalling 2020 AMG CLA 35 and 2021 GLA 250 vehicles because loose rear brake caliper fasteners may reduce braking performance or cause parts to detach.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250, AMG CLA35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V126000·2022-03-04

    Midwest Automotive Designs Recalls 2018-2020 Sprinter Vans Due to Fire Risk

    Midwest Automotive Designs is recalling 2018-2020 Passage, Weekender, and Daycruiser Sprinter Vans because a circuit board may overheat and cause a fire.

    Product
    MIDWEST AUTOMOTIVE DESIGN — MIDWEST AUTOMOTIVE DESIGN PASSAGE, WEEKENDER, DAYCRUISER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V127000·2022-03-04

    2022 Kia Sorento Vehicles Recalled for Seatbelt Pretensioner Defect

    Kia is recalling 2022 Sorento Hybrid and Sorento PHEV vehicles because the front seatbelt pretensioner(s) may explode during a crash, potentially projecting metal fragments at occupants. Dealers will replace the pretensioners at no cost.

    Product
    KIA — KIA SORENTO HYBRID, SORENTO PHEV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V128000·2022-03-04

    Hino Recalls 2022 NJ7A Trucks Due to Air Brake Fastener Issue

    Hino is recalling 2022 NJ7A vehicles because an improperly tightened air compressor nut may cause low air pressure, potentially triggering the parking brake and increasing crash risk.

    Product
    HINO — HINO NJ7A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V123000·2022-03-03

    2022 Hyundai Elantra and Elantra HEV Seat Belt Pretensioner Explosion Hazard

    Hyundai is recalling 2022 Elantra and Elantra HEV vehicles because the front passenger-side seat belt pretensioner may explode during a crash, projecting metal fragments that could strike and injure vehicle occupants.

    Product
    HYUNDAI — HYUNDAI ELANTRA, ELANTRA HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V121000·2022-03-03

    Motorhome tire valve stem may lose pressure, increasing crash risk

    Jayco and Entegra motorhomes from 2018–2023 may have defective tire valve stem extensions that contact the wheel rim, causing damage and potential tire pressure loss that increases crash risk.

    Product
    ENTEGRA — ENTEGRA, JAYCO ACCOLADE, ACCOLADE XL, SENECA PRESTIGE, SENECA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22E016000·2022-03-03

    Pony.ai Recalls Automated Driving Systems Due to Software Shutdown Risk

    Pony.ai is recalling specific Automated Driving Systems (ADS) because a software error may cause the system to shut down unexpectedly while the vehicle is moving.

    Product
    ELECTRICAL SYSTEM:ADAS:AUTONOMOUS/SELF DRIVING:SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide