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.

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.

36551–36575 of 77447

  • SevereFDA (Drugs)·D-0770-2019·2019-03-20

    King Bio Recalls Dr. King's SafeCare Rx Candida Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Candida bottles due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Candida, 8 fl. oz. (236 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955620686, NDC 57955-6207-8
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0609-2019·2019-03-20

    King Bio Homeopathic Hair & Nails Formula Recalled for Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Hair & Nails Formula due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Hair & Nails Formula, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955504924, NDC 57955-5049-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0950-2019·2019-03-20

    King Bio Para Solve Homeopathic Liquid Recalled for Microbial Contamination

    King Bio Inc. is recalling NET Remedies #6 Para Solve Homeopathic Preparation due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    NET Remedies #6 Para Solve Homeopathic Preparation, Oral Liquid, 57 mL, NDC 57955-4206-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0732-2019·2019-03-20

    King Bio Recalls Anti-Aging Cream Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's SafeCare Rx Anti-Aging & Wrinkles For Men due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's SafeCare Rx Anti-Aging & Wrinkles For Men, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Drive, Asheville, NC 28806 USA, UPC 357955714729, NDC 57955-7148-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0557-2019·2019-03-20

    King Bio Recalls Homeopathic Arnica Due to Microbial Contamination

    King Bio Inc. is recalling Dr. King's Natural Medicine Homeopathic Advanced Arnica due to microbial contamination. The product was distributed in the U.S., Canada, and Australia.

    Product
    Dr. King's Natural Medicine Homeopathic Advanced Arnica, 2 fl. oz. (59 mL), King Bio, Inc., 3 Westside Dr. Asheville, NC 28806, UPC 357955598428, NDC 57955-5984-2
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1006-2019·2019-03-20

    FDA Recalls NexGen Trabecular Metal Tibial Augments Due to Labeling Mismatch

    Zimmer Trabecular Metal Technology is recalling 26 units of NexGen Trabecular Metal Tibial Half Block Augments because the product in the box may not match the label.

    Product
    NexGenTrabecular Metal Tibial Half Block Augment, Left Lateral/Right Medial, Size 4 5MM Thickness W/Screws Item Number: 00544800436 Product Usage: The Trabecular Metal Tibial Cone Augments are intended for use where severe degeneration, trauma, or other pathology of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·19730·2019-03-20

    Kubota Recalls Zero Turn Mowers Due to Fire Hazard

    Kubota is recalling about 3,850 zero turn mowers because the throttle cable can contact internal wiring, posing a fire hazard. No injuries have been reported.

    Product
    Kubota Zero Turn Mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·19V221000·2019-03-20

    Osage Ambulances Recalled for Brake Lights Illuminating Without Pedal Press

    Osage is recalling 2015-2019 Brave, Warrior, and Super Warrior ambulances because brake lights may illuminate when the brake pedal is not pressed, potentially confusing other drivers.

    Product
    OSAGE — OSAGE BRAVE, WARRIOR, SUPER WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·19088·2019-03-20

    Honda Recalls Portable Generators Due to Fire and Burn Hazards

    American Honda is recalling approximately 200,000 portable generators because a fuel valve leak can cause fire and burn hazards. No injuries have been reported.

    Product
    Honda EU2200i, EU220i Companion and EB2200i Portable Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0994-2019·2019-03-20

    Durex Pleasure Pack Condoms Recalled for Burst Pressure Failure

    Reckitt Benckiser is recalling Durex Pleasure Pack condoms because five batches failed burst pressure specifications.

    Product
    Durex Pleasure Pack (60 ct), synthetic polisoprene male condom, SKU 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00 02340-98729-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1167-2019·2019-03-20

    Nature's Path Organic Chocolate Choco Chimps Cereal Recalled for Undeclared Gluten

    Nature's Path is recalling Organic Chocolate Choco Chimps cereal because it may contain undeclared gluten (wheat and barley).

    Product
    Nature's Path Organic Chocolate Choco Chimps Organic cereal. Net Wt. 10 oz (284 g), UPC 58449-87024. Nature's Path Foods, Inc., Blaine, WA 98230
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V218000·2019-03-20

    Volkswagen Atlas and Passat Recall for Incorrect Side Air Bags

    Volkswagen is recalling 2019 Atlas and 2020 Passat vehicles because incorrect side air bags may have been installed, potentially failing to deploy in a crash.

    Product
    VOLKSWAGEN — VOLKSWAGEN ATLAS, PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0993-2019·2019-03-20

    Durex Real Feel Condoms Recalled for Burst Pressure Failure

    Reckitt Benckiser LLC is recalling Durex Real Feel condoms because five batches failed burst pressure specifications.

    Product
    Durex Real Feel, synthetic polisoprene male condom, SKU 02340-89456-14 02340-89455-00 02340-89456-14 02340-89456-14 02340-89455-00 02340-95767-00 02340-89456-14 02340-89457-00 02340-89456-14 02340-89456-14 02340-89455-00 02340-89455-00 02340-95767-00 02340-95767-00
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·19V215000·2019-03-20

    Thor Motor Coach Recalls 2018-2019 Quantum RW28 Motorhomes for Missing Lights

    Thor Motor Coach is recalling 2018-2019 Quantum RW28 motorhomes because they may be missing mid-ship marker lights, which can cause other drivers to underestimate the vehicle's length.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH QUANTUM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0996-2019·2019-03-20

    Steris Recalls AMSCO 5000 Series Washer/Disinfector Units Due to Software Defect

    Steris Corporation is recalling 68 AMSCO 5000 Series Washer/Disinfector units because a software defect may prevent the intended cleaning cycle from processing, potentially leading to inadequate disinfection.

    Product
    AMSCO 5000 Series Washer/Disinfector Model # 5052
    Category
    Medical Device
    Distribution
    27 states
  • HighFDA (Food)·F-1168-2019·2019-03-20

    Nature's Path Organic Gorilla Munch Corn Puffs Recalled for Undeclared Gluten

    Nature's Path is recalling Organic Gorilla Munch Corn Puffs cereal because it may contain undeclared gluten (wheat and barley). The recall covers 23,969 cases distributed nationwide and internationally.

    Product
    Nature's Path Organic Gorilla Munch Corn Puffs cereal. Net Wt. 10 oz (284 g), UPC 58449-86002. Nature's Path Foods, Inc., Blaine, WA 98230.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V214000·2019-03-20

    Fouts Bros Fire Apparatus Recall for Brake Light Wiring Defect

    Fouts Bros is recalling 2017-2018 F-3000, F-Rescue, and F-Pumper fire apparatus vehicles because brake lights may illuminate without the brake pedal being pressed.

    Product
    FOUTS BROS. — FOUTS BROS. F-PUMPER, F-3000, F-RESCUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1169-2019·2019-03-20

    Nature's Path Organic Cinnamon Jungle Munch Recalled for Undeclared Gluten

    Nature's Path is recalling Organic Cinnamon Jungle Munch cereal because it may contain undeclared gluten (wheat and barley).

    Product
    Nature's Path Organic Cinnamon Jungle Munch cereal. Net Wt. 10 oz (284 g), UPC 58449-87028. Nature's Path Foods, Inc., Blaine, WA 98230.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1011-2019·2019-03-20

    US Endoscopy Padlock Clip Recalled for Potential Esophageal Laceration Risk

    US Endoscopy Group Inc is recalling Padlock Clip defect closure systems due to a risk of esophageal laceration during patient procedures.

    Product
    US Endoscopy Padlock Clip defect closure system Ref: C910001 The Padlock Clip is indicated for use in flexible endoscopy and for the compression of tissue in the gastrointestinal tract, for hemostasis or for treating lesions of the wall of the gastrointestinal organs.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0995-2019·2019-03-20

    Steris Recalls AMSCO 3000 Series Washer/Disinfector Units Due to Software Defect

    Steris Corporation is recalling 11 AMSCO 3000 Series Washer/Disinfector units because a software defect may prevent intended processing cycles, risking inadequate cleaning or damage to medical instruments.

    Product
    AMSCO 3000 Series Washer/Disinfector Model # 3052
    Category
    Medical Device
    Distribution
    27 states
  • ModerateFDA (Food)·F-1157-2019·2019-03-20

    Kradjian Importing Recalls Zarrin Pickled Cucumbers Due to Leaking Cans

    Kradjian Importing Co is recalling Zarrin Pickled Cucumbers & Cornichons because some cans are leaking and swollen. Consumers should stop using the product.

    Product
    Zarrin Pickled Cucumbers & Cornichons: Net Weight 101.4 oz. 3 kg. Ingredients: Cucumber, water, salt, acid (acetic acid, spices, food coloring (tartrazine). Refrigerate after opening. UPC 7 64363 18305 2 Product of the West Bank Packed for Blanish International, PO Box…
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Food)·F-1158-2019·2019-03-20

    Kradjian Imports Recalls Leaking and Swollen Bulgarian White Brined Sheep's Milk Cheese

    Kradjian Imports Co. is recalling 952 cases of Bulgarian White Brined Sheep's Milk cheese due to leaking and swollen cans. The product was distributed across 14 states.

    Product
    Bulgarian White Brined Sheep's Milk cheese; 5 gallon can Ingredients: Pasteurized Sheep's Milk, Bacterial culture, salt, rennet. Product of Belgium. Imported by Kradjian Imports Co., Inc., Glendale, CA 91204
    Category
    Food
    Distribution
    14 states
  • ModerateFDA (Devices)·Z-1010-2019·2019-03-20

    Olympus TJF-Q180V Duodenoscope Recalled Due to Adhesive Preparation Error

    Olympus is recalling two TJF-Q180V duodenoscopes because the adhesive used in their repair was incorrectly prepared, potentially affecting the device's durability or effectiveness.

    Product
    Olympus TJF-Q180V Duodenoscope - Product Usage: These endoscopes are intended for use in endoscopic diagnosis and treatment within the gastrointestinal tract.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1003-2019·2019-03-20

    Ossur ReSolve Halo Vest Recalled for Labeling and Safety Testing Issues

    Ossur Americas is recalling 381 ReSolve Halo Vests because the titanium pin label incorrectly lists a ceramic tip and the products require confirmatory safety testing.

    Product
    Ossur, ReSolve Halo Vest, Part/ Description: 545700K/ ReSolve Halo Vest-shrt kodel; 545700L/ ReSolve Halo Vest-shrt lmbwool; 545800K/ ReSolve Halo Vest-tall kodel; 545800L/ ReSolve Halo Vest-tall lmbwool
    Category
    Medical Device
    Distribution
    28 states