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.

35751–35775 of 77447

  • HighFDA (Devices)·Z-1177-2019·2019-04-24

    ProSun V3 42 Tanning Beds Recalled for Potential High UV Output

    ProSun International is recalling nine specific tanning beds due to quality control documentation discrepancies that could result in high UV output.

    Product
    ProSun V3 42 Xlc(160w)(10 minutes) tanning bed, Model 500. Labeled as the following: PROSUN V3 42 HIGH INTENSIVE (160W) PEARL WHITE (TMAX READY), PROSUN V3 42 HIGH INTENSIVE (160W) PEARL WHITE, PROSUN V3 42 HIGH INTENSIVE (160W) RED, PROSUN V3 42 HIGH INTENSIVE (160W) PEARL…
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1196-2019·2019-04-24

    Abbott Alinity i Processing Module Recalled for Safety Interlock Defect

    Abbott is recalling Alinity i Processing Modules because a safety interlock may fail to deploy when a bulk solution bottle is removed.

    Product
    Abbott Alinity i Processing Module LN 03R65-01 - Product Usage: The Alinity i processing module is a fully automated immunoassay analyzer allowing random and continuous access, as well as priority and automated retest processing using chemiluminescent microparticle immunoassay…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1150-2019·2019-04-24

    Integra Salto Talaris Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Salto Talaris and Integra XT Revision ankle implants because the labels list an incorrect metallic coating material symbol.

    Product
    Salto Talaris, Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Right, Part No. LJU200T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Food)·F-1293-2019·2019-04-24

    Wholesome Treats Recalls Breads from Anna Dairy and Corn Free Bread Mix

    Wholesome Treats, Inc. is recalling Breads from Anna Dairy & Corn Free Bread Mix because the product contains undeclared flaxseed.

    Product
    Breads from Anna Dairy & Corn Free Bread Mix 19oz, carton
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1173-2019·2019-04-24

    Integra Talar Dome Total Ankle Prosthesis Recalled for Labeling Error

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Left, Product No. LJV191T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Drugs)·D-1123-2019·2019-04-24

    InvaGen Recalls Testosterone Cypionate Injection Due to Particulate Matter

    InvaGen Pharmaceuticals is recalling specific lots of Testosterone Cypionate Injection because they contain particulate matter.

    Product
    TESTOSTERONE CYPIONATE — TESTOSTERONE CYPIONATE (TESTOSTERONE CYPIONATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1138-2019·2019-04-24

    Topcon IMAGEnet 6 Software Recalled for Patient Data Display Error

    Topcon Medical Systems is recalling IMAGEnet 6 software due to a defect that may display incorrect patient identification information alongside thumbnails.

    Product
    IMAGEnet 6 v1.53- IMAGEnet 6 Ophthalmic Data System is a software program that is intended for use in the collection, storage and management of digital images, patient data, diagnostic data and clinical information from Topcon devices without controlling or altering the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1166-2019·2019-04-24

    Integra Talar Dome Total Ankle Prosthesis Recalled for Labeling Error

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis , Flat Cut, Size 2, Right, Product No. LJU812T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1175-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis , Sloped, Size 3, Left, Product No. LJV193T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1168-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels incorrectly identify the metallic coating material.

    Product
    Talar Dome Total Ankle Prosthesis , Sloped, Size 0, Right, Product No. LJV180T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1174-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Labeling Error

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels incorrectly list the metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis, Sloped, Size 2, Left, Product No. LJV192T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1171-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels incorrectly identify the metallic coating material.

    Product
    Talar Dome Total Ankle Prosthesis , Sloped, Size 3, Right, Product No. LJV183T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1169-2019·2019-04-24

    Integra LifeSciences Recalls Talar Dome Ankle Prostheses Due to Labeling Error

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis , Sloped, Size 1, Right, Product No. LJV181T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1141-2019·2019-04-24

    Philips Medical Systems Recalls Foot Switches for Allura Xper Systems

    Philips Medical Systems is recalling 7,209 foot switches used with Allura Xper systems because pedals may bend, causing an inability to make live fluoroscopy images or exposures.

    Product
    Foot Switches used with the following systems: 722001 Allura Xper FD 10 C 722002 Allura Xper FD10 F 722003 Allura Xper FD10 722005 Allura Xper FD10/10 722006 Allura Xper FD20 722008 Allura Xper FD20 Biplane 722010 Allura Xper FD10 722011 Allura Xper FD10/10 722012…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1135-2019·2019-04-24

    Ethicon Recalls VICRYL Plus Sutures Due to Labeling Mismatches

    Ethicon, Inc. is recalling VICRYL Plus Sutures because the product may not match the sales unit carton and foil label.

    Product
    VICRYL PLUS Sutures: VICRYL PLUS SUTURE 18"(45CM) 3-0 VIO VICRYL PLUS SUTURE 18"(45CM) 0 UND VICRYL PLUS SUTURE 18"(45CM) 0 VIO VICRYL PLUS SUTURE 18"(45CM) 0 VIO) VICRYL PLUS SUTURE 18"(45CM) 1 VIO VICRYL PLUS SUTURE 18"(45CM) 4-0 VIO VICRYL PLUS SUTURE 27"(70CM) 3-0…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1154-2019·2019-04-24

    Salto Talaris Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Salto Talaris Tibial Total Ankle Prosthesis trays due to incorrect metallic coating material symbols on labels and instructions.

    Product
    Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 0, Left, Part No. LJU210T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1160-2019·2019-04-24

    Integra Tibial Total Ankle Prosthesis Tray Recalled for Labeling Errors

    Integra LifeSciences is recalling Tibial Total Ankle Prosthesis Trays due to incorrect metallic coating symbols on labels and instructions.

    Product
    Tibial Total Ankle Prosthesis Tray, Size 2, Product No. LJU222T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Food)·F-1292-2019·2019-04-24

    Wholesome Treats Recalls Breads from Anna Yeast Free Bread Mix

    Wholesome Treats, Inc. is recalling Breads from Anna Yeast Free Bread Mix because the product contains undeclared flaxseed, which is not listed on the label.

    Product
    Breads from Anna Yeast Free Bread Mix 18.1oz, carton
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1158-2019·2019-04-24

    Integra Tibial Total Ankle Prosthesis Tray Recalled for Labeling Error

    Integra LifeSciences Corp. is recalling Tibial Total Ankle Prosthesis Trays because the labels list an incorrect metallic coating material symbol.

    Product
    Tibial Total Ankle Prosthesis Tray, Size 0, Product No. LJU220T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1152-2019·2019-04-24

    Integra Recalls Salto Talaris Ankle Prosthesis Due to Labeling Error

    Integra LifeSciences is recalling Salto Talaris Tibial Total Ankle Prosthesis trays because the labels list an incorrect metallic coating material symbol.

    Product
    Salto Talaris Tibial Total Ankle Prosthesis Tray, Talar Dome, Size 2, Right, Part No. LJU202T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1167-2019·2019-04-24

    Integra Talar Dome Ankle Prosthesis Recalled for Incorrect Labeling

    Integra LifeSciences is recalling Talar Dome Total Ankle Prostheses because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Talar Dome Total Ankle Prosthesis, Flat Cut, Size 3, Right, Product No. LJU813T
    Category
    Medical Device
    Distribution
    26 states
  • ModerateFDA (Devices)·Z-1161-2019·2019-04-24

    Integra Tibial Total Ankle Prosthesis Tray Recalled for Labeling Error

    Integra LifeSciences Corp. is recalling Tibial Total Ankle Prosthesis Trays because the labels and instructions for use list an incorrect metallic coating material symbol.

    Product
    Tibial Total Ankle Prosthesis Tray, Size 3, Product No. LJU223T
    Category
    Medical Device
    Distribution
    26 states