The Recall Desk

State

US Virgin Islands product recalls

73,388 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
177
Critical
12
Severe
39
Most recent
2026-09-23

Of the 177 recalls naming US Virgin Islands we have scored against our rubric, 12 (7%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 39 (22%) are Severe.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

22226–22250 of 73565

  • 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
  • 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·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, CHARGER, BIGHORN
    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
    PRIME TIME — PRIME TIME, FOREST RIVER, CONTINENTAL CARGO SANIBEL, CARDINAL, CRUSADER, CONTINENTAL CARGO
    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
  • HighCPSC·22715·2022-01-06

    Children's Covered Wood Wagons Recalled for Excessive Lead Paint

    Colony Brands is recalling about 20 covered wood wagons sold through Montgomery Ward's and Ginny's from September to October 2021 because paint on the wood, plastic handles, and red plastic cover contains excessive lead that can be toxic if ingested by young children.

    Product
    Covered Wood Wagons
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-0363-2022·2022-01-05

    kleantouch Hand Sanitizer recalled for methanol contamination

    Valisa MFG LLC is recalling kleantouch Hand Sanitizer 8 FL OZ pump bottles nationwide because the product contains methanol and was marketed without FDA approval. Consumers should stop using the product immediately.

    Product
    kleantouch HAND SANITIZER (ethyl alcohol 70%), 8.0 FL OZ (236 ML), pump bottles, Distributed by: Valisa MFG, LLC, Farmingdale, NY, 11735, Made in USA, UPC 6 86162 99246 1
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0323-2022·2022-01-05

    SterRx Phenylephrine HCl Injection Recalled for Sterility Assurance

    SterRx is recalling PHENYLephrine HCl 40 mg per 250 mL injectable solution nationwide due to lack of assurance of sterility. The recall affects approximately 20,640 bags distributed across the United States.

    Product
    PHENYLephrine HCl, 40 mg per 250 mL, (160 mcg per mL) in 0.9% Sodium Chloride Injection, Rx Only, SterRx, 141 Idaho Ave., Plattsburgh, NY 12903, NDC 70324-252-01.
    Category
    Drug
    Distribution
    Distributed nationwide