State

Colorado product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

24301–24325 of 80513

ModerateFDA (Drugs)·D-0339-2022·2022-01-12
H.E.B Allergy Relief Fexofenadine tablets recalled for impurity specification failure
Perrigo Company is recalling H.E.B Allergy Relief fexofenadine hydrochloride 60mg tablets nationwide due to failure of impurity specifications during stability testing.
Product
H.E.B Allergy Relief, Fexofenadine Hydrochloride tablets, 12HR, 60mg/Antihistamine 12 count bottle, Made with Pride & Care for H.E.B. San Antonio TX 78204, Product of Czech Republic, NDC 37808-425-53, UPC 0 41220 53080 9
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0361-2022·2022-01-12
Pregabalin Capsules Recalled for Out-of-Specification Manufacturing Defects
Sun Pharmaceutical Industries is recalling Pregabalin 50 mg capsules due to out-of-specification results in particle size distribution and bulk density of the active pharmaceutical ingredient.
Product
PREGABALIN — PREGABALIN (PREGABALIN)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0348-2022·2022-01-12
Rite Aid Allergy Relief Fexofenadine tablets recalled for impurity
Perrigo Company PLC is recalling Rite Aid Allergy Relief Fexofenadine Hydrochloride 180mg tablets nationwide due to failed impurity specifications. An out-of-specification result for impurity A was found during stability testing.
Product
Rite Aid ALLERGY RELIEF Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, packaged as a) 30 count bottle, NDC 11822-0571-2 UPC 0 11822 99908 3; b) 150 count bottle, NDC 11822-0571-5 UPC 0 11822 85411 5; Made in the Czech Republic, Distributed by Rite Aid 30 Hunter…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0331-2022·2022-01-12
Perrigo basic+care Fexofenadine Tablets Recall—Failed Impurity Specifications
Perrigo Company PLC is recalling basic+care allergy Fexofenadine Hydrochloride Tablets (180 mg, 150-count bottles) distributed nationwide because impurity testing results exceeded specification limits during stability testing.
Product
basic+care, allergy Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24 HR, 150 count bottle, Made in the Czech Republic, Distributed by: Perrigo Allergan, MI 49010, NDC 0113-7571-47 UPC 3 70030 11470 2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0359-2022·2022-01-12
Cefixime Capsules 400 mg Recalled for Failed Impurities and Degradation
Ascend Laboratories recalls Cefixime 400 mg capsules due to failed impurities and degradation specifications. The affected 42,698 bottles were distributed nationwide.
Product
CEFIXIME — CEFIXIME (CEFIXIME)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0332-2022·2022-01-12
Fexofenadine Hydrochloride Tablets Recall for Failed Impurity Specifications
Perrigo Company PLC is recalling basic+care allergy Fexofenadine Hydrochloride Tablets, 60 mg, 100-count bottles, due to out-of-specification impurity levels detected during stability testing.
Product
basic+care, allergy Fexofenadine Hydrochloride Tablets, 60 mg/Antihistamine, 12HR, 100 count bottle, Made in the Czech Republic, Distributed by: Perrigo Allergan, MI 49010, NDC 0113-7425-78 UPC 3 70030 14536 2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0354-2022·2022-01-12
Amazon Basic+Care Fexofenadine Tablets Recalled for Failed Impurity Specifications
Amazon Basic+Care Allergy Fexofenadine Hydrochloride Tablets (60 mg, 100-count) are being recalled because impurity levels exceeded acceptable limits during stability testing. The recall affects 38,352 bottles distributed nationwide.
Product
amazon basic+care, Allergy Fexofenadine Hydrochloride Tablets, 60 mg/Antihistamine, 12HR, 100 count bottle, Made in the Czech Republic, Distributed by: Amazon.com services LLC 410 Terry Avenue N., Seattle WA 98109, NDC 72288-425-78 UPC 3 70030 14536 2
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0350-2022·2022-01-12
TopCare Allergy Relief Fexofenadine tablets recalled for impurity specifications
Perrigo Company PLC is recalling TopCare Allergy Relief Fexofenadine Hydrochloride 180mg tablets in multiple pack sizes due to failed impurity specifications during stability testing. The affected lots were distributed nationwide.
Product
TopCare Allergy Relief, Fexofenadine Hydrochloride tablets, 24HR, 180mg Antihistamine, packaged as a) 5 count bottle, NDC 36800-319-13 UPC 0 36800 33277-5 b) 15 count bottle, NDC 36800-319-22 UPC 0 36800 33278 2; c) 45 count bottle, NDC 36800-319-95 UPC 0 36800 33280-5; d) 90…
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0337-2022·2022-01-12
Health Mart Fexofenadine Tablets Recalled for Failed Impurity Specifications
Perrigo Company PLC is recalling Health Mart Fexofenadine Hydrochloride 12HR 60mg tablets due to impurity A exceeding specification limits during stability testing. The recall affects 12,384 containers distributed nationwide.
Product
Health Mart, Fexofenadine Hydrochloride tablets, 12HR, 60mg . Antihistamine 12 count bottle, Distributed by: Mckesson 6555 State Highway 161, Irvine, TX 75039. Made in the Czech Republic, NDC 62011-0413-1, UPC 0 52569 14278 3
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0330-2022·2022-01-12
Amazon Allergy Fexofenadine Hydrochloride Tablets Recalled for Failed Impurity Specifications
Amazon-branded Allergy Fexofenadine Hydrochloride Tablets 180 mg are being recalled because testing found an out-of-specification impurity during stability testing.
Product
amazon, Allergy Fexofenadine Hydrochloride Tablets, 180 mg/Antihistamine, 24 HR, 30 count bottle, Made in the Czech Republic, Distributed by: Amazon.com Services LLC 410 Terry Avenue N. Seattle, WA 98109 UPC 3 70030 11466 5
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0335-2022·2022-01-12
CVS Allergy Relief Fexofenadine Tablets Recalled for Impurity
CVS Allergy Relief Fexofenadine Hydrochloride Tablets 60 mg are being recalled because stability testing found an out-of-specification result for impurity A. The recall affects approximately 138,144 containers distributed nationwide.
Product
CVS Allergy Relief, Fexofenadine Hydrochloride Tablets, 60 mg Antihistamine, 12HR, packaged as a) 12 count bottle, NDC 59779-425-53, UPC 0 50428 25414 1; b)24 count bottle, NDC 59779-425-62, UPC 0 50428 53435 9; Distributed by: CVS Pharmacy, Inc. One CVS Drive, Woonsocket, RI…
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·22V009000·2022-01-11
Oshkosh Recalls 2019-2022 S-Series Vehicles Due to Front Axle Bolt Failure Risk
Oshkosh is recalling 2019-2022 S-Series vehicles because front axle u-bolts may fail, potentially allowing the axle to shift or detach and increasing crash risk.
Product
OSHKOSH — OSHKOSH S-SERIES
Category
Vehicle
Distribution
Distributed nationwide
SevereCPSC·22045·2022-01-11
Bella Residential Elevators Recalled for Child Entrapment Hazard
Bella residential elevators pose a risk of child entrapment between exterior and interior doors. Young children can become trapped and suffer serious injuries or death when the elevator moves to another floor.
Product
Bella residential elevators
Category
Consumer Product
Distribution
Distributed nationwide
SevereCPSC·22047·2022-01-11
Residential Elevators Recalled for Child Entrapment Hazard
Savaria and Garaventa residential elevators pose an entrapment risk to young children due to gaps between doors. Young children can become trapped and suffer serious injury or death when the elevator is called to another floor.
Product
Savaria and Garaventa branded residential elevators
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V007000·2022-01-11
Play-Mor Trailers Recalled Due to Propane Regulator Fire Risk
Play-Mor is recalling specific 2017-2020 trailers because a propane regulator may fail, increasing pressure and fire risk. Dealers will replace the parts free of charge.
Product
PLAY-MOR — PLAY-MOR MOTORSPORT SUV TRAILER, SINGLE ROOM TRAILER, 2 ROOM TRAILER, BBQ TRAILER
Category
Vehicle
Distribution
Distributed nationwide
HighCPSC·22046·2022-01-11
Inclinator residential elevators recalled for child entrapment hazard
Inclinator Company of America is recalling residential elevators manufactured from 1979 through 2021 because young children can become entrapped between the exterior landing door and interior elevator car door, risking serious injury or death.
Product
Inclinator residential elevators
Category
Consumer Product
Distribution
Distributed nationwide
HighNHTSA·22V008000·2022-01-11
Oshkosh Recalls 2019-2022 S-Series Vehicles Due to Fuel Leak Fire Risk
Oshkosh is recalling 2019-2022 S-Series vehicles because fuel tubes may crack, causing high-pressure leaks that increase fire risk.
Product
OSHKOSH — OSHKOSH S-SERIES
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V006000·2022-01-10
Reading Truck Recalls Marauder Dump Bodies Due to Weld Failure Risk
Reading Truck Body is recalling 2017-2021 Marauder Landscape Dump Body vehicles because a rear pivot mount weld may fail, increasing injury risk.
Product
READING TRUCK — READING TRUCK MARAUDER DUMP
Category
Vehicle
Distribution
Distributed nationwide
SevereUSDA FSIS·003-2022·2022-01-08
Abbyland Foods Recalls Beef Sticks for Undeclared Milk Allergen
Abbyland Foods is recalling approximately 14,976 pounds of smoked beef sticks because they contain undeclared milk, a known allergen.
Product
Abbyland Foods, Inc. Recalls Beef Stick Product Due to Misbranding and Undeclared Allergens
Category
Food
Distribution
Distributed nationwide
SevereNHTSA·22V005000·2022-01-07
Lakota Recalls 2021-2022 Trailers Due to Tire Belt Separation Risk
Lakota is recalling 2021-2022 Bighorn, Charger, and Livestock trailers because certain tires may experience belt separation, increasing crash risk.
Product
LAKOTA — LAKOTA LIVESTOCK, BIGHORN, CHARGER
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V003000·2022-01-07
2022 Forest River Aurora travel trailers recalled for furnace cooktop fire risk
Forest River is recalling 2021-2022 Aurora and Catalina travel trailers because the panel sealing the cooktop from the furnace was not properly sealed, which could cause an inverted flame and fire risk.
Product
COACHMEN — COACHMEN, FOREST RIVER CATALINA, AURORA
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·22V004000·2022-01-07
2022 Forest River Cardinal Trailers Recalled for Tire Belt Separation
Forest River, Inc. is recalling certain 2021-2022 fifth wheel trailers equipped with defective Sailun tires that may experience belt separation. The defect could cause loss of vehicle control and increase the risk of a crash.
Product
CONTINENTAL CARGO — CONTINENTAL CARGO, PRIME TIME, FOREST RIVER CONTINENTAL CARGO, CRUSADER, SANIBEL, CARDINAL
Category
Vehicle
Distribution
Distributed nationwide
CriticalUSDA FSIS·001-2022·2022-01-06
Interstate Meat Dist. Recalls Ground Beef Due To E. Coli O157:H7
Interstate Meat Dist. Inc. is recalling approximately 28,356 pounds of ground beef products due to possible E. coli O157:H7 contamination.
Product
Interstate Meat Dist. Inc., Recalls Ground Beef Products Due To Possible E. Coli O157:H7 Contamination
Category
Food
Distribution
Distributed nationwide
HighCPSC·22716·2022-01-06
Polaris Outlaw 110 EFI Youth ATVs Recalled for Fire Hazard
Polaris is recalling about 1,100 Model Year 2022 Outlaw 110 EFI Youth ATVs because the inner layer of the fuel line can leak, posing a fire hazard. No fires or injuries have been reported.
Product
Outlaw 110 EFI Youth All-Terrain Vehicles (ATVs)
Category
Vehicle
Distribution
Distributed nationwide
HighUSDA FSIS·002-2022·2022-01-06
Kettle River Recalls Chicken Alfredo Pizza for Undeclared Wheat Allergen
Kettle River Products is recalling approximately 1,464 pounds of chicken alfredo pizza due to misbranding and an undeclared wheat allergen. No adverse reactions have been reported.
Product
Kettle River Products Recalls Chicken Alfredo Pizza Products Due to Misbranding and an Undeclared Allergen
Category
Food
Distribution
Distributed nationwide