The Recall Desk

State

US Virgin Islands product recalls

73,722 recalls have nationwide distribution and so reach US Virgin Islands. 178 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
178
Critical
12
Severe
39
Most recent
2026-10-21

Of the 178 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.

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,722 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

33526–33550 of 73900

  • SevereNHTSA·19V431000·2019-06-08

    Farber Specialty Vehicles Recalls 2018 XCR Models Due to Brake Bolt Issue

    Farber Specialty Vehicles is recalling 2018 XCR specialty vehicles because brake caliper mounting bolts may not be sufficiently tightened, which can reduce brake effectiveness and increase crash risk.

    Product
    FCCC — FCCC XCR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V425000·2019-06-07

    Mazda Recalls 2019 Mazda3 Vehicles Due to Loose Lug Nuts

    Mazda is recalling 2019 Mazda3 vehicles because lug nuts may loosen, potentially causing a wheel to detach and increasing crash risk.

    Product
    MAZDA — MAZDA MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·066-2019·2019-06-07

    Tyson Recalls Chicken Fritters Due to Possible Hard Plastic Contamination

    Tyson Foods is recalling approximately 190,757 pounds of ready-to-eat chicken fritters that may contain hard plastic. The products were shipped to institutional foodservice locations nationwide.

    Product
    Tyson Foods, Inc. — Tyson Foods, Inc. Recalls Ready-To-Eat Chicken Fritter Products due to Possible Foreign Matter Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighNHTSA·19V429000·2019-06-07

    Mickey Truck Bodies Recalls 2017-2018 Ford F-750 Vehicles

    Mickey Truck Bodies is recalling 2017-2018 Ford F-750 vehicles because back-up camera monitors may revert to factory settings, causing the image to reverse and increasing crash risk.

    Product
    FORD — FORD F-750
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V426000·2019-06-07

    Newmar Recalls Motorhomes Due to Rear Light Malfunction Risk

    Newmar is recalling specific 2016-2019 motorhomes because a damaged power module may cause rear lights to fail, increasing crash risk.

    Product
    NEWMAR — NEWMAR MOUNTAIN AIRE, DUTCH STAR, ESSEX, VENTANA LE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V430000·2019-06-07

    Morgan Olson P31 Recalled for Reversed Backup Camera Image

    Morgan Olson is recalling 2018 P31 vehicles because backup camera monitors may revert to factory settings, causing the image to reverse and increasing crash risk.

    Product
    MORGAN OLSON — MORGAN OLSON P31
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·065-2019·2019-06-06

    Table 87 Frozen Recalls Pork Pizza Produced Without Federal Inspection

    Table 87 Frozen, LLC is recalling approximately 649 pounds of frozen prosciutto pizzas produced without federal inspection. No adverse reactions have been reported.

    Product
    Table 87 Frozen, LLC — Table 87 Frozen, LLC Recalls Pork Pizza Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V424000·2019-06-06

    Acura Recalls 2016-2019 ILX Vehicles for Driveshaft Separation Risk

    Acura is recalling 2016-2019 ILX vehicles because excessive grease may prevent a set-ring from engaging, allowing the driveshaft to separate and increase crash risk.

    Product
    ACURA — ACURA ILX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·19V422000·2019-06-06

    2020 International HV Trucks Recalled for Wheel Bearing Lubrication Defect

    Navistar is recalling 2020 International HV Severe Service Diesel Trucks because insufficient steer axle hub lubrication may cause wheel bearing damage and potential wheel separation.

    Product
    INTERNATIONAL — INTERNATIONAL HV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V421000·2019-06-06

    Land Rover Recalls 2020 Range Rover Evoque for Washer Fuse Failure

    Jaguar Land Rover is recalling 2020 Range Rover Evoque vehicles because a fuse failure may reduce driver visibility, increasing crash risk.

    Product
    LAND ROVER — LAND ROVER RANGE ROVER EVOQUE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V423000·2019-06-06

    SkyMark Recalls 2018 Flowmark Vacuum Trucks Due to Monitor Defect

    SkyMark Refuelers is recalling 2018 Flowmark Vacuum Trucks because the back-up camera monitors may revert to factory settings, reversing the image and increasing crash risk.

    Product
    FLOWMARK — FLOWMARK VACUUM TRUCK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·19V419000·2019-06-06

    Diamond Coach VIP 2800 Recalled for Reversed Backup Camera Image

    Diamond Coach is recalling one 2017 VIP 2800 vehicle because the backup camera display may revert to factory settings, causing the image to reverse and increasing crash risk.

    Product
    DIAMOND COACH — DIAMOND COACH VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Drugs)·D-1321-2019·2019-06-05

    Stiff Boy LLC Recalls The Beast Due to Undeclared Sildenafil

    Stiff Boy LLC is recalling The Beast because FDA analysis found undeclared sildenafil. The product was marketed without an approved NDA or ANDA.

    Product
    The Beast, The Beast can be taken under the situation of Heart disease and even after drinking, 4600 mg X 4 Capsules per packet.
    Category
    Drug
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-1443-2019·2019-06-05

    Laxmi Brand Dried Apricots Recalled for Undeclared Sulfites

    House of Spices India, Inc. is recalling Laxmi Brand Dried Apricots because the product contains elevated levels of undeclared sulfites.

    Product
    Laxmi Brand Dried Apricot 7 oz (200g) Plastic Pouch UPC Code: 2324617054
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1573-2019·2019-06-05

    Maquet Getinge Adult ECC Pack Recall Due to Sterility Assurance Concerns

    Maquet Cardiovascular is recalling Adult ECC Packs because a design feature may prevent sterilization gas from reaching all fluid paths, potentially compromising sterility.

    Product
    Maquet Getinge-BO-TOP 36504 ADULT ECC PACK Material: 701065765
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1519-2019·2019-06-05

    Maquet Custom Tubing Sets Recalled Due to Sterility Assurance Concerns

    Maquet Cardiovascular is recalling custom tubing sets for extracorporeal circulation because a design feature may prevent sterilization gas from reaching all fluid paths.

    Product
    Maquet Getinge-BEQ-TOP 27901 SMALL PATIENT CI Material:701052287
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1526-2019·2019-06-05

    Maquet Getinge Custom Tubing Sets Recalled for Sterility Assurance Concerns

    Maquet Cardiovascular is recalling specific custom tubing sets for extracorporeal circulation because a design flaw may prevent proper sterilization of the stopcock ports.

    Product
    Maquet Getinge-BO-TOP 20705 SMALL PATIENT 1/4 Material: 701053486
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1537-2019·2019-06-05

    Maquet Getinge ECC Tubing Sets Recalled for Sterility Assurance Concerns

    Maquet Cardiovascular is recalling specific ECC tubing sets because a design feature may prevent proper sterilization, potentially compromising sterility.

    Product
    Maquet Getinge-BEQ-T 8025 1/4" ECC Pack with RF32 Material:701055142
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1547-2019·2019-06-05

    Maquet Getinge ECC Tubing Sets Recalled Due to Sterility Assurance Concerns

    Maquet Cardiovascular is recalling specific batches of Getinge-BEQ-TOP 38900 ECC Packs because a design flaw may prevent proper sterilization of the stopcock ports.

    Product
    Maquet Getinge-BEQ-TOP 38900 ECC PACK Material: 701056368
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1511-2019·2019-06-05

    Maquet Getinge-BEQ-TOP Circulatory Circuits Recalled for Sterility Assurance Concerns

    Maquet Cardiovascular is recalling specific batches of Maquet Getinge-BEQ-TOP 15704 Circulatory Circuits because a design feature may prevent proper sterilization of the stopcock ports.

    Product
    Maquet Getinge-BEQ-TOP 15704 Circulatory Circuit 3/8" Material: 701050859
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1376-2019·2019-06-05

    Terumo Portico Solo Re-Collapsible Access System Recalled for Tip Dislodgement

    Terumo Medical Corporation is recalling Portico Solo Re-Collapsible Access Systems because the tip may dislodge from the sheath, potentially causing injury.

    Product
    Portico Solo Re-Collapsible Access System , Model Numbers PRTSOLO-19, PRTSOLO-20
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-1308-2019·2019-06-05

    Avella Recalls Bevacizumab Prefilled Syringes Due to Sterility Concerns

    Avella of Deer Valley, Inc. is recalling 730 prefilled syringes of Bevacizumab 2.5 mg/0.1 mL due to a lack of assurance of sterility.

    Product
    Bevacizumab 2.5 mg/0.1 mL, packaged in a Prefilled Syringe, Rx only, AVELLA SPECIALTY PHARMACY 24416 N. 19TH AVENUE PHOENIX, AZ 85085, NDC 42852-001-27
    Category
    Drug
    Distribution
    Distributed nationwide