The Recall Desk

State

New Mexico product recalls

72,966 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 72,966 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

3426–3450 of 76591

  • HighCPSC·26256·2026-02-05

    Ammunition desiccant tiles recalled over failure to control humidity

    About 760 Ammo Tabs fiber desiccant tiles are being recalled because they can fail to protect firearms and ammunition from humidity, allowing corrosion or rust.

    Product
    Ammo Tabs Fiber Desiccant Tiles used for Firearms and Ammunition
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26238·2026-02-05

    Six drawer dressers recalled over tip-over and entrapment hazards

    About 600 Shintenchi 6-drawer dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.

    Product
    Shintenchi 6-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26248·2026-02-05

    Seven drawer dressers recalled over tip-over and entrapment hazards

    About 2,900 Fixwal 7-Drawer Dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.

    Product
    Fixwal 7-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26255·2026-02-05

    Ten drawer dressers recalled over tip-over and entrapment hazards

    About 5,000 EnHomee 10-Drawer Dressers are being recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards to children.

    Product
    EnHomee 10-Drawer Dressers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26240·2026-02-05

    Youth hooded clothing recalled over drawstrings that pose strangulation risk

    About 620 items of Lola + The Boys hooded clothing with drawstrings are being recalled because the drawstrings can catch on objects, posing a strangulation hazard to children.

    Product
    Lola + The Boys Youth Clothing with Drawstrings
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26254·2026-02-05

    Toddler busy books recalled over beads that can detach

    About 3,500 Cobelae Busy Books for toddlers are being recalled because beads on page eight can loosen and detach, posing a choking hazard.

    Product
    Cobelae Busy Book for Toddlers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·26249·2026-02-05

    LED Christmas headbands recalled over accessible button cell batteries

    About 250 Dresbe LED Christmas Headbands are being recalled because children can easily access the button cell batteries and the product lacks the warnings required by Reese's Law.

    Product
    Dresbe LED Christmas Headbands
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0433-2026·2026-02-04

    Super greens powder tubs recalled over possible Salmonella Typhimurium contamination

    Superfoods, Inc. is recalling Live it Up brand Super Greens powder, net weight 8.5oz, because the products may be contaminated with Salmonella Typhimurium.

    Product
    Live it Up brand Super Greens; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 8.5OZ (240G); Manufactured for Superfoods, Inc.; UPC: 860013190804 b.) Live it Up brand Super Gr
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·H-0434-2026·2026-02-04

    Super greens powder recalled over possible Salmonella Typhimurium contamination

    Superfoods, Inc. is recalling 795,834 units of Live it Up brand Super Greens because the products may be contaminated with Salmonella Typhimurium.

    Product
    a.) Live it Up brand Super Greens; Natural Wild Berry Flavor; Chlorella, Spirulina, Wheatgrass, Kale, Broccoli, Spinach, Barley grass, Moringa, Parsley; Whole food dietary supplement powder; 30 day supply; NET WT. 9.49oz (269.16g); Manufactured for Superfoods, Inc.; UPC: 86001319
    Category
    Food
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1115-2026·2026-02-04

    Broselow Rainbow Tape 7700RE recalled over potentially harmful dosing errors

    SunMed Holdings is recalling 20,583 units of the Broselow Pediatric Emergency Rainbow Tape, model 7700RE, because it contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.

    Product
    Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700RE Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1117-2026·2026-02-04

    Filled Broselow organizers recalled over potentially harmful dosing errors

    SunMed Holdings is recalling 89 units of the Filled Broselow Organizer, model 7730IALS, because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.

    Product
    Brand Name: Broselow Product Name: BROSELOW" FILLED BROSELOW ORGANIZER Model/Catalog Number: 7730IALS Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care. Comp
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-1114-2026·2026-02-04

    Pediatric emergency tapes recalled over potentially harmful drug dosing errors

    SunMed Holdings is recalling 95,300 units of the Broselow Pediatric Emergency Rainbow Tape because the product contains potentially harmful dosing errors for Vecuronium, Flumazenil and Ketamine.

    Product
    Brand Name: Broselow Product Name: Broselow Pediatric Emergency Rainbow Tape Model/Catalog Number: 7700REA Software Version: Not Applicable Product Description: The Broselow Tape is a length- and weight-based reference tool specifically designed for pediatric emergency care.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1203-2026·2026-02-04

    Chest drainage units recalled to limit their use to adults

    Cardinal Health is updating the instructions for use on 1,169,726 chest drainage units to clarify that the intended patient population is adults 18 years and older.

    Product
    Chest Drainage Units and Accessories: Product Code Description 1. 8888571562 Cardinal Health Sentinel Seal CDU 2. 8888571513 Cardinal Health Sentinel Seal CDU, Dual Drain 3. 8888571489 Cardinal Health Sentinel Seal CDU, with Easy Change Connector 4. 8888571370 Cardinal
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·26252·2026-02-04

    Combination fuel containers recalled over missing flame mitigation devices

    About 700 Scepter B62 gas and oil combination fuel containers are being recalled because they lack flame mitigation devices and the spout is not child-resistant.

    Product
    Scepter Gas and Oil Combination Fuel Containers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1182-2026·2026-02-04

    Feminine hygiene products recalled over rodent activity in a distribution center

    Gold Star Distribution is recalling feminine hygiene products over potential exposure of rodents and rodent activity in its distribution center.

    Product
    Feminine hygiene products, labeled as: KOTEX FREEDOM MAXI NO WINGS 48CT, ALWAYS THIN LINERS UNSCENTED 12 CT, ALWAYS THIN LINERS SCENTED 12CT, ALWAYS ULT.THIN WINGS REG.12/22CT, ALWAYS ULT.THIN OVER NIGHT WINGS 12/16CT, JULIE MAXI NIGHT W.WINGS 36/10CT, STAY FREE REG. 12/10CT
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1170-2026·2026-02-04

    Lemon ginger hibiscus beer recalled over possibly unpasteurized ginger juice

    Weaver's Brew is recalling 1,014 cases of Goldenroot Lemon Ginger Hibiscus Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.

    Product
    Genesis Knotless Anchor
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1181-2026·2026-02-04

    Condoms recalled over rodent activity in a distribution center

    Gold Star Distribution is recalling condoms over potential exposure of rodents and rodent activity in its distribution center.

    Product
    Condoms, labeled as: TROJAN MAGNUM CONDOMS 6/DSP BLACK, TROJAN LUBRICATED CONDOMS 6/DSP LITE BLUE, TROJAN SPERMICIDE CONDOMS 6/DSP DARK BLUE, TROJAN ULTRA THIN CONDOMS 6/DSP GREY, TROJAN RIBBED CONDOMS 6/DSP GOLD/BROWN, TROJAN NONLUBRICATED CONDOMS 6/DSP RED, TROJAN ULTRA HER
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1186-2026·2026-02-04

    Lemon ginger jalapeno beer recalled over possibly unpasteurized ginger juice

    Weaver's Brew is recalling 421 cases of Goldenroot Lemon Ginger Jalapeno Ginger Beer because the products might contain ginger juice that did not undergo the required pasteurization process.

    Product
    Medline medical procedure convenience kits labeled as: NERVE BLOCK TRAY 2, Kit SKU DYNJRA2713
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1168-2026·2026-02-04

    Screw-in suture anchors recalled after reports of breakage and bending

    Aju Pharm is recalling 600 units of the Genesis Screw-In Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    Genesis Screw-In Anchor
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1213-2026·2026-02-04

    Hybrid suture anchors recalled after reports of breakage and pull out

    Aju Pharm is recalling 233 units of the Fixone Hybrid Anchor after reports of device failure including anchor breakage, bending, pull out and suture breakage.

    Product
    MR 7700. Product Code (REF): (1) 782120, (2) 782153. MR systems with SW version R11.1 and R12.1.
    Category
    Medical Device
    Distribution
    Distributed nationwide