The Recall Desk

State

Colorado product recalls

73,388 recalls have nationwide distribution and so reach Colorado. 6,945 additional recalls listed Colorado specifically in their distribution scope.

What the numbers show

Total
6,945
Critical
1,218
Severe
1,823
Most recent
2026-10-02

Of the 6,945 recalls naming Colorado we have scored against our rubric, 1,218 (18%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 1,823 (26%) are Severe.

These figures cover only the 6,945 recalls whose distribution notice names Colorado specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19601–19625 of 80333

  • HighNHTSA·22V909000·2022-12-08

    School buses recalled for incorrectly tightened rear axle fasteners

    Navistar is recalling certain 2023-2024 IC BUS school buses due to fasteners on the rear axle that may have been tightened incorrectly. This can allow the rear axle to shift, reducing vehicle control and increasing crash risk.

    Product
    IC BUS — IC BUS CESB, RESB, EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V903000·2022-12-08

    GM recalls multiple 2020-2023 vehicles for daytime running light control defect

    General Motors is recalling multiple 2020-2023 models because daytime running lights may fail to turn off when headlights are on, creating glare and visibility hazards.

    Product
    BUICK — BUICK, GMC, CADILLAC ENVISION, SIERRA 1500, YUKON, YUKON XL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateCPSC·23063·2022-12-08

    Life is Good Darkest Blue Fleece Sweatshirts and Shorts Recall

    The Life is Good Company is recalling approximately 750 Fall 2022 Darkest Blue fleece sweatshirts and men's shorts that fail to meet federal flammability standards for clothing textiles, posing a risk of burn injuries.

    Product
    Fall 2022 Darkest Blue Fleece Women's Sweatshirts and Men's Shorts
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0354-2023·2022-12-07

    Alcon Surgical Procedure Packs Recalled for Adhesive Defect and Skin Injuries

    Alcon is recalling Custom Pak Surgical Procedure Packs because the adhesive liner is difficult to remove and the manufacturer has observed an increase in skin injuries related to the adhesive.

    Product
    Alcon Custom Pak Surgical Procedure Pack
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0347-2023·2022-12-07

    Medical laboratory reagent recalled for potential false-negative test results

    Greer Laboratories recalled a hypersensitivity pneumonitis test reagent (Lot 389591) due to decreased reactivity that could cause false-negative results. The issue affects 218 units distributed across 12 U.S. states and two countries.

    Product
    GREER M. FAENI, 0.25 mL 20 MG/ML, Item: K6, Analyte Specific Reagent, HYPERSENSITIVITY PNEUMONITIS test system, gel diffusion kit for demonstrating precipitating antibodies.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Devices)·Z-0344-2023·2022-12-07

    Mobile CT Scanner Battery Fire Risk in Units With Bypassed Monitoring

    Mobius Imaging is recalling MobiCT-32 AIRO Mobile CT Scanner units due to a reported battery fire in devices where battery monitoring systems were bypassed. The affected units' batteries must be replaced.

    Product
    MobiCT-32 AIRO Mobile CT Scanner, Cat. No. MobiCT-32, mobile computed tomography (CT) system, software version 2.1.1
    Category
    Medical Device
    Distribution
    3 states
  • HighFDA (Devices)·Z-0340-2023·2022-12-07

    Intuitive Da Vinci Stapler Instruments Recalled for Potential Staple Deployment Failure

    Intuitive Surgical is recalling Da Vinci Xi surgical stapling instruments due to potential staple deployment failure and device fragment generation. No injuries have been reported.

    Product
    INTUITIVE Da Vinci Xi 8mm SureForm 30 Curved-Tip Stapler Da Vinci Xi|X REF 488530 INTUITIVE Da Vinci 8mm SureForm 30 Reload 30 mm Gray 4-Row 2.0 mm Xi|X REF 48230M INTUITIVE Da Vinci 8mm SureForm 30 Reload 30 mm White 4-Row 2.5 mm Xi|X REF 48230W INTUITIVE Da Vinci 8mm…
    Category
    Medical Device
    Distribution
    24 states
  • HighFDA (Devices)·Z-0342-2023·2022-12-07

    CMV IgM EIA Diagnostic Test Recalled for Increased False Positives

    Bio-Rad Laboratories is recalling 180 CMV IgM EIA diagnostic test kits due to unusually high rates of false positive results. The recall affects test kits distributed in 14 U.S. states.

    Product
    CMV IgM EIA, in vitro diagnostic.
    Category
    Medical Device
    Distribution
    14 states
  • HighNHTSA·22V902000·2022-12-07

    Nova Bus Recalls LFS Models for Non-Standard Auxiliary Lighting

    Nova Bus is recalling 2009-2021 LFS and LFS Artic transit buses because non-standard color auxiliary lights may distract other drivers and increase crash risk.

    Product
    NOVA BUS — NOVA BUS LFS, LFS ARTIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0072-2023·2022-12-07

    FDA recalls prescription desmopressin acetate tablets for subpotency

    Heritage Pharmaceuticals' desmopressin acetate tablets (0.2mg) have been recalled nationwide due to subpotency. The voluntary recall affects 13,805 bottles; no illnesses have been reported.

    Product
    DESMOPRESSIN ACETATE — DESMOPRESSIN ACETATE (DESMOPRESSIN ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0348-2023·2022-12-07

    Medical device test system recalled for decreased reactivity and false-negative results

    Greer Laboratories recalled a hypersensitivity pneumonitis test kit (102 units, Lot 389592) after stability testing revealed decreased reactivity that could cause false-negative results. The issue was discovered in October 2021.

    Product
    GREER DIA - KIT ANTIGEN M. FAENI, 2.0mL 20 MG/ML, Analyte Specific Reagent, Item: K62, HYPERSENSITIVITY PNEUMONITIS test system, gel diffusion kit for demonstrating precipitating antibodies.
    Category
    Medical Device
    Distribution
    11 states
  • HighFDA (Drugs)·D-0071-2023·2022-12-07

    Daytrana transdermal methylphenidate patches recalled for adhesive defect

    Noven Pharmaceuticals recalls 3,977 boxes of Daytrana methylphenidate transdermal patches nationwide due to defective adhesive properties in lot 91316. Affected patches may fail to adhere properly or deliver medication inconsistently.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0179-2023·2022-12-07

    Coolhaus Dairy Free Frozen Dessert Recalled for Coliform Detection

    Coolhaus Dairy Free Cookie Dough Lyfe frozen dessert sandwiches recalled due to coliform detected in lab samples. Product distributed to select retailers in Texas, Maryland, Colorado, and California.

    Product
    Coolhaus Dairy Free Cookie Dough Lyfe Frozen Dessert Sandwich 3 pk units - 8.75 oz (2.9 oz./unit) UPC: 8 5000988328 5 Distributed by Coolhaus 8688 Washington Blvd. Culver City, CA 90232
    Category
    Food
    Distribution
    4 states
  • ModerateNHTSA·22V901000·2022-12-07

    Audi Recalls 2023 S3, RS3, and A3 for Missing Weight Label

    Volkswagen Group of America is recalling 2023 Audi S3, RS3, and A3 vehicles because the B-pillar safety label is missing weight capacity information.

    Product
    AUDI — AUDI S3, RS 3, A3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0074-2023·2022-12-07

    Acella Recalls Sodium Sulfacetamide Cleansing Pads for Subpotency

    Acella Pharmaceuticals is recalling Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads because testing found the drug out of specification for potency at shelf-life expiration. 528 cartons distributed nationwide are affected.

    Product
    Sodium Sulfacetamide 10% Sulfur 4% Cleansing Pads, Net weight 3.7g (60 cleansing pads Net weight 3.7 g each per carton,) Rx Only, Manufactured For: Acella Pharmaceuticals, LLC Alpharetta, GA 300025, NDC 42192-113-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0073-2023·2022-12-07

    Allergy Relief D tablets recalled for failed dissolution specifications

    Dr. Reddy's Laboratories is recalling Allergy Relief D extended-release tablets distributed nationwide by Walmart due to failed dissolution specifications. No illnesses or injuries have been reported.

    Product
    Allergy Relief D, Fexofenadine HCL 60mg/Antihistamine, Pseudoephedrine HCL 120mg/Nasal Decongestant, Extended-Release Tablets USP, packaged as (a) 20 count carton NDC 49032-273-20; (b) 30 count carton, NDC49032-273-30; Distributed by: Walmart Inc., Bentonville, AR 72716, Product…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V899000·2022-12-06

    Kia Recalls 2020 Niro EV Vehicles for EPCU Coolant Leak Risk

    Kia is recalling 2020 Niro EV vehicles because a coolant leak in the Electric Power Control Unit may cause loss of drive power, increasing crash risk.

    Product
    KIA — KIA NIRO EV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V898000·2022-12-06

    Hino Recalls 2022-2023 Trucks Due to Fuel Pickup Tube Defect

    Hino is recalling 970 specific 2022-2023 models because a fuel tube may restrict fuel flow, potentially causing engine stalls and increasing crash risk.

    Product
    HINO — HINO NJ7A, NJ7B, NV7A, NE7A
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V900000·2022-12-06

    KTM 1290 Super Duke R Motorcycles Recalled for Electrical Wiring Defect

    KTM is recalling 2020-2022 1290 Super Duke R motorcycles because the main wiring harness may be misrouted or missing parts, potentially causing an electrical short-circuit and engine stall.

    Product
    KTM — KTM 1290 SUPER DUKE R
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V896000·2022-12-06

    Volvo Recalls 2022-2023 VNL Vehicles for Air Tank Bracket Defect

    Volvo Trucks is recalling certain 2022-2023 VNL vehicles because excessively tightened air tank bracket fasteners may break, allowing the air tank to detach and become a road hazard.

    Product
    VOLVO — VOLVO VNL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V895000·2022-12-05

    Tesla Recalls 2023 Model Y Vehicles for Suspension Fastener Defect

    Tesla is recalling 2023 Model Y vehicles because front suspension fasteners may not be properly attached, which could cause instability and increase crash risk.

    Product
    TESLA — TESLA MODEL Y
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22T022000·2022-12-05

    Continental Tire Recalls Specific Models Due to Sidewall Break Risk

    Continental Tire is recalling specific 4x4 Contact, PureContact LS, and TerrainContact H/T tires because overcuring may cause sidewall breaks or tread separation, increasing crash risk.

    Product
    TIRES:SIDEWALL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide