The Recall Desk

State

Colorado product recalls

73,509 recalls have nationwide distribution and so reach Colorado. 6,947 additional recalls listed Colorado specifically in their distribution scope.

What the numbers show

Total
6,947
Critical
1,218
Severe
1,823
Most recent
2026-10-14

Of the 6,947 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.

Which agencies issued them

These figures cover only the 6,947 recalls whose distribution notice names Colorado specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

23576–23600 of 80456

  • ModerateFDA (Drugs)·D-0602-2022·2022-03-02

    Good Sense Children's Pain and Fever acetaminophen oral suspension recall

    Perrigo is recalling Good Sense Children's Pain and Fever acetaminophen oral suspension (160 mg/5 ml) in 4 FL OZ bottles due to contaminated excipient used during manufacturing. The recalled batch 1CK0963 (expiration 12/31/2022) was distributed nationwide.

    Product
    GOOD SENSE CHILDRENS PAIN AND FEVER — GOOD SENSE CHILDRENS PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0583-2022·2022-03-02

    Acetaminophen Child Strawberry Suspension Recalled for Contaminated Excipient

    Perrigo Company PLC is recalling Acetaminophen Child Strawberry Oral Suspension (160 mg/5 ml) due to use of a contaminated excipient. The product was manufactured with a recalled ingredient from the excipient supplier.

    Product
    Acetaminophen Child Strawberry Oral Suspension (160 mg/5 ml), 4 FL OZ (118 mL) per bottle, Distributed by: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015. NDC: 0363-0971-26
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0647-2022·2022-03-02

    Premium Nature Instant Hand Sanitizer Recalled for Subpotent Ethanol

    AMS Packaging Inc is recalling Premium Nature Instant Hand Sanitizer (70% ethyl alcohol) in 8 oz and 16 oz bottles because some bottles contain less ethanol than labeled, reducing effectiveness.

    Product
    Premium Nature Instant Hand Sanitizer, (ethyl alcohol 70%), plastic bottle packaged as (a) 8 OZ, UPC 8 19192 02866 8; (b) 16 OZ, UPC 8 19192 02874 3; Premium Nature, South Plainfield, NJ.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0598-2022·2022-03-02

    Equate Infant Pain and Fever Acetaminophen Recall Due to Contaminated Excipient

    Perrigo Company is recalling Equate infant's acetaminophen oral suspension due to manufacturing deviations involving a contaminated excipient from a supplier. The product was distributed nationwide.

    Product
    EQUATE PAIN AND FEVER — EQUATE PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0656-2022·2022-03-02

    Medline Michels Transport Medium Recalled for Improper Storage Conditions

    Medline is recalling 2,816 Michels Transport Medium prefilled containers due to improper storage in a temperature-controlled setting instead of refrigeration.

    Product
    Michels Transport Medium, 20ML Prefilled Cont
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0616-2022·2022-03-02

    DG Health Nasal Spray Recalled for Contaminated Excipient

    Perrigo Company is recalling DG Health Nasal (Oxymetazoline Hydrochloride) nasal spray because it was manufactured with a contaminated excipient obtained from a recalled supplier.

    Product
    DG HEALTH NASAL — DG HEALTH NASAL (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0613-2022·2022-03-02

    Basic Care No Drip Nasal Spray Recalled for Contaminated Excipient

    Perrigo Company is recalling 1,296 bottles of Basic Care No Drip Nasal Spray (oxymetazoline hydrochloride 0.05%) distributed nationwide due to contaminated excipient used during manufacturing.

    Product
    BASIC CARE NO DRIP NASAL — BASIC CARE NO DRIP NASAL (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0623-2022·2022-03-02

    Equaline Nasal Oxymetazoline HCl Nasal Spray Recalled for Contaminated Excipient

    Perrigo Company PLC is recalling 1,560 bottles of Equaline Nasal No Drip Nasal Spray nationwide due to contaminated excipient used during manufacturing. The contaminated ingredient was sourced from a recalled excipient supplier.

    Product
    EQUALINE NASAL — EQUALINE NASAL (OXYMETAZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0579-2022·2022-03-02

    Acetaminophen Oral Suspension Recalled for Contaminated Excipient

    Perrigo is recalling Acetaminophen Oral Suspension Grape Flavor (160 mg/5 mL, 16 fl oz bottles) nationwide because the product was manufactured with a contaminated excipient that was recalled by the excipient supplier.

    Product
    Acetaminophen Oral Suspension Grape Flavor, 160 mg per 5 mL, 16 fl oz (473 mL) per bottle, Distributed by Perrigo, Allegan, MI 49010. NDC: 50941-009-43
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0628-2022·2022-03-02

    Nasal Spray Oxymetazoline HCl Recalled Due to Contaminated Excipient

    Perrigo Company PLC is recalling Nasal Maximum Strength Nasal Spray (Oxymetazoline HCl 0.05%) due to contamination from a recalled excipient used during manufacturing. Approximately 2,302 bottles were distributed nationwide.

    Product
    NASAL — NASAL (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0580-2022·2022-03-02

    Equate Children's Pain and Fever Acetaminophen Suspension Recall

    Perrigo Company is recalling Equate Children's Pain and Fever Acetaminophen Suspension (160mg/5ml) due to contaminated excipient used in manufacturing. Approximately 117,552 bottles distributed nationwide are affected.

    Product
    EQUATE CHILDRENS PAIN AND FEVER — EQUATE CHILDRENS PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0625-2022·2022-03-02

    TOPCARE NASAL Oxymetazoline HCl Recalled Due to Contaminated Excipient

    Perrigo Company PLC is recalling TOPCARE NASAL (Oxymetazoline HCl 0.05%) nasal spray nationwide because products were manufactured with a contaminated excipient obtained from a supplier whose material was recalled.

    Product
    TOPCARE NASAL — TOPCARE NASAL (OXYMETAZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0608-2022·2022-03-02

    Nasal Oxymetazoline Spray Recalled for Contaminated Excipient

    Perrigo Company is recalling approximately 9,888 bottles of NASAL Severe Congestion Nasal Spray due to contamination from a recalled excipient used during manufacturing. The product was distributed nationwide.

    Product
    NASAL — NASAL (OXYMETAZOLINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0597-2022·2022-03-02

    Parents Choice Infant Acetaminophen Recalled for Contaminated Excipient

    Perrigo Company is recalling approximately 55,656 bottles of Parents Choice Infants Pain and Fever (Acetaminophen) oral suspension nationwide due to CGMP deviations. The product was manufactured with a contaminated excipient that was recalled from the supplier.

    Product
    PARENTS CHOICE INFANTS PAIN AND FEVER — PARENTS CHOICE INFANTS PAIN AND FEVER (ACETAMINOPHEN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0615-2022·2022-03-02

    Nasal Mist Oxymetazoline HCl Recalled for Contaminated Excipient

    Perrigo Company PLC is recalling approximately 64,512 bottles of NASAL MIST oxymetazoline nasal decongestant distributed nationwide because they were manufactured with a contaminated excipient recalled from the supplier.

    Product
    NASAL MIST — NASAL MIST (OXYMETAZOLINE HCL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·22E015000·2022-03-01

    Marion Body Works Recalls Emergency Vehicles Due to Fuel Leak Risk

    Marion Body Works is recalling specific 2018-2021 emergency vehicles because a fuel rail defect may cause leaks, increasing fire risk.

    Product
    MARION BODY WORKS — MARION BODY WORKS FREIGHTLINER M2, KENWORTH T3 SERIES, INTERNATIONAL SR525
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighUSDA FSIS·PHA-03012022-01·2022-03-01

    Ready-to-Eat Meat Products Recalled for Undeclared Wheat Allergen

    USDA FSIS issued a public health alert for ready-to-eat meat products containing a seasoning mix with undeclared wheat. Consumers are advised not to consume these items.

    Product
    FSIS Issues Public Health Alert for Ready-to-Eat Meat Products Containing FDA-Regulated Seasoning Mix That Has Been Recalled Due to Misbranding and an Undeclared Allergen
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·22V116000·2022-03-01

    Pierce Arrow XT Firetruck Recall for Improperly Crimped Lifting Cables

    Pierce Manufacturing is recalling one 2021 Arrow XT firetruck because improperly crimped lifting cables could cause the generator set to fall, increasing injury risk.

    Product
    PIERCE — PIERCE ARROW XT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V114000·2022-02-28

    Proterra buses recalled for loose steering gearbox securing bolts

    Proterra is recalling 2017-2022 Catalyst and ZX5 buses because steering gearbox securing bolts may loosen due to insufficient adhesive, risking loss of steering control. Owner notifications were sent October 7, 2022.

    Product
    PROTERRA — PROTERRA ZX5, CATALYST
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V112000·2022-02-25

    Mercedes-Benz Recalls 2022 EQS Models Due to Electrical Fire Risk

    Mercedes-Benz is recalling 2022 EQS 450, EQS 580, and AMG EQS 53 vehicles because improperly secured electrical connections may increase the risk of a fire or cause headlight failure.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ EQS 580, EQS 450, AMG EQS 53
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V109000·2022-02-24

    Ford Recalls 2021 Escape Hybrid Vehicles Due to Crankshaft Defect

    Ford is recalling 2021 Escape Hybrid vehicles because an incorrectly manufactured engine crankshaft may cause engine damage, leading to stalling or fire.

    Product
    FORD — FORD ESCAPE HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V108000·2022-02-24

    Tenco Recalls One TOR DR-106100 Highway Carrier for Fuel Leak Risk

    Tenco Inc. is recalling one 2020 TOR DR-106100 highway carrier because fuel tubes may crack, causing a high-pressure fuel leak that increases fire risk.

    Product
    TOR — TOR DR-106100
    Category
    Vehicle
    Distribution
    Distributed nationwide