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.

37026–37050 of 77447

  • ModerateFDA (Devices)·Z-0804-2019·2019-02-13

    Richard Wolf Bronchoscope Tubes Recalled for Potential Bonding Defects

    Richard Wolf GmbH is recalling 873 Bronchoscope Tubes, Model Texas, because non-functional bonding points may loosen. The devices are used for respiratory tract investigation and therapy.

    Product
    Richard Wolf Bronchoscope Tubes, Model Texas. Device is reusable and should be sterilized prior to each use. Product Usage: Bronchoscopes are intended for investigation, diagnosis and therapy of pathological changes and removal of foreign bodies in the area of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0427-2019·2019-02-13

    Medline Remedy Barrier Ointment Recalled for Microbial Contamination

    US Pharmaceuticals is recalling Medline Remedy Barrier Skin Protectant Ointment due to out-of-specification microbial counts in purified water.

    Product
    Medline Remedy Essential Barrier Skin Protectant Ointment (petrolatum 59%) packaged in a) 2 oz tubes (NDC 53329-302-14) and b) 6 oz tubes (NDC 53329-302-41), Medline Industries Inc., Manufactured for Medline Industries Inc., Mundelien, IL 60060.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0815-2019·2019-02-13

    Angiotech Recalls Bone Marrow Biopsy Needles Due to Sterile Seal Defect

    Angiotech is recalling 1,260 bone marrow biopsy needles due to a manufacturing issue affecting the sterile seal on blister trays.

    Product
    J Type Bone Marrow Needle 13ga x 10 cm- Product Usage: Manual surgical instruments for Bone Marrow Biopsy and Aspiration.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0818-2019·2019-02-13

    Bone Marrow Biopsy Needle Recall Due to Sterile Seal Manufacturing Issue

    Angiotech is recalling 1,404 Bone Marrow Biopsy Needles due to a manufacturing defect in the sterile seal on blister trays.

    Product
    Aguja de Aspiracion con Profundidad Ajustable Tipo I 16ga x 5 cm- Product Usage: Manual surgical instruments for Bone Marrow Biopsy and Aspiration.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0426-2019·2019-02-13

    US Pharmaceuticals Recalls Hydrocortisone Cream Due to Microbial Contamination

    US Pharmaceuticals is recalling Hydrocortisone Cream Intensive Healing due to out-of-specification microbial counts in purified water.

    Product
    HYDROCORTISONE CREAM INTENSIVE HEALING — HYDROCORTISONE CREAM INTENSIVE HEALING (HYDROCORTISONE CREAM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0799-2019·2019-02-13

    Abbott Recalls ARCHITECT Total T3 Reagent Kits Due to Carryover

    Abbott Ireland Diagnostics Division is recalling ARCHITECT Total T3 Reagent Kits because reagent carryover may cause depressed test results on specific platforms.

    Product
    ARCHITECT Total T3 Reagent Kit used on ARCHITECT i1000SR or i2000/i2000SR platforms Product Usage: It is a Chemiluminescent Microparticle Immunoassay (CMIA) for the quantitative determination of free triiodothyronine (Free T3) in human serum and plasma.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0819-2019·2019-02-13

    Bone Marrow Biopsy Needle Recall Due to Sterile Seal Manufacturing Issue

    Angiotech is recalling 2,502 bone marrow biopsy needles due to a manufacturing issue affecting the sterile seal on blister trays.

    Product
    Aguja para Biopsia Tipo Medula Osea Ergonomica 11ga x 10cm
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0429-2019·2019-02-13

    Lupin Recalls Bimatoprost Ophthalmic Solution Due to Impurity Failures

    Lupin Pharmaceuticals is recalling Bimatoprost Ophthalmic Solution 0.03% because out-of-specification results were observed for individual and total impurities.

    Product
    Bimatoprost Ophthalmic Solution 0.03%, packaged in a) 5 mL (NDC 68180-429-02) and b) 7.5 mL (NDC 68180-429-03) bottles, Rx only, Manufactured by: Lupin Limited Pithampur (M.P.) 454 775, INDIA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V093000·2019-02-12

    Freightliner Cascadia Recall for Tie-Rod Failure Risk

    Daimler Trucks North America is recalling 2013-2016 Freightliner Cascadia trucks because brake vibrations may cause tie-rod failure, leading to loss of steering.

    Product
    FREIGHTLINER — FREIGHTLINER CASCADIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19062·2019-02-12

    Target Recalls Toddler Unicorn Boots Due to Choking Hazard

    Target is recalling Cat & Jack toddler boots because the unicorn horn can detach, posing a choking hazard to children.

    Product
    Cat & Jack Unicorn "Chiara" Boots
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V078000·2019-02-11

    Forest River Recalls 2019 Columbus Trailers Due to Hitch Bolt Issue

    Forest River is recalling 2019 Columbus recreational trailers because insufficiently tightened pin box mounting bolts could cause the trailer to separate from the tow vehicle.

    Product
    FOREST RIVER — FOREST RIVER COLUMBUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V081000·2019-02-11

    Blue Bird Recalls One 2019 Vision Bus for Wheelchair Lift Defect

    Blue Bird is recalling one 2019 Vision bus because a wheelchair lift component may fail, allowing the platform to rise too high and increasing injury risk.

    Product
    BLUE BIRD — BLUE BIRD VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V080000·2019-02-11

    Lakota Recalls 2018-2019 Trailers Due to Incorrect Tire Placard Data

    Lakota is recalling 2018-2019 Bighorn, Charger, Colt, and Livestock Edition trailers because incorrect tire data on the Federal Placard could lead to tire overload and failure.

    Product
    LAKOTA — LAKOTA BIGHORN, CHARGER, COLT, LIVESTOCK EDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V082000·2019-02-11

    Blue Bird Recalls School Buses with Defective Wheelchair Lifts

    Blue Bird is recalling 2015-2019 Vision and All American school buses because a wheelchair lift component may fail, causing the platform to rise too high and increasing the risk of injury.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V085000·2019-02-08

    Forest River Cherokee Recalled for Incorrect Federal Tire Placard Information

    Forest River is recalling 2019 Cherokee recreational trailers because the Federal Placards list incorrect tire size information, which may lead to the installation of insufficient tires.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V064000·2019-02-08

    Isuzu and Chevrolet Trucks Recalled for Odometer Unit Display Error

    Isuzu is recalling 2019 NPR and Chevrolet 4500/5500 trucks because the odometer may display kilometers instead of miles, potentially delaying critical maintenance.

    Product
    CHEVROLET — CHEVROLET, ISUZU LOW CAB FORWARD 4500, NRR, LOW CAB FORWARD 5500, NPR HD
    Category
    Vehicle
    Distribution
    Distributed nationwide