The Recall Desk

State

US Virgin Islands product recalls

73,570 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.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26826–26850 of 73748

  • SevereFDA (Drugs)·D-0081-2021·2020-11-25

    Hand Sanitizer Recalled for Methanol Contamination and Low Ethanol Content

    Albek De Mexico is recalling Assured Instant Hand Sanitizer bottles because they contained methanol and had lower ethanol levels than labeled.

    Product
    Assured Instant Hand Sanitizer Vitamin E and Aloe (Ethyl Alcohol 70% v/v), 8 fl oz/ 237 mL bottle, Distributed By: Greenbrier International, Inc. 500 Volvo Parkway, Chesapeake, VA 23320. Made in Mexico, UPC 639277928597
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0097-2021·2020-11-25

    Ascent Pharmaceuticals Recalls Hydrocodone and Acetaminophen Tablets Due to Foreign Tablet

    Ascent Pharmaceuticals is recalling 9,768 bottles of Hydrocodone Bitartrate and Acetaminophen Tablets because one bottle contained a Losartan Potassium tablet.

    Product
    Hydrocodone Bitartrate and Acetaminophen Tablets, USP 10 mg/325mg 100-count bottles, Rx Only, Manufactured for : Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, Manufactured by: Ascent Pharmaceuticals, Inc. Central Islip, NY 11722, NDC 31722-943-01
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0080-2021·2020-11-25

    Assured Instant Hand Sanitizer Recalled for Methanol Contamination

    Albek De Mexico S.A. De C.V. is recalling 27,000 bottles of Assured Instant Hand Sanitizer because the product contained methanol and was below the label claim for ethanol content.

    Product
    Assured Instant Hand Sanitizer Aloe & Moisturizers (Ethyl Alcohol 70% v/v) 8 fl oz / 237 mL bottle, Distributed By: Greenbrier International, Inc. 500 Volvo Parkway, Chesapeake, VA 23320. Made in Mexico.UPC 639277928610
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V739000·2020-11-25

    Peterbilt 520 Recalled for Incorrect Brake Relay Connections

    PACCAR is recalling 2020-2021 Peterbilt 520 vehicles because incorrectly connected brake components may destabilize the vehicle during stability control events, increasing crash risk.

    Product
    PETERBILT — PETERBILT 520
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0082-2021·2020-11-25

    Next Advanced Antibacterial Hand Sanitizer Recalled for Methanol Contamination

    Albek De Mexico S.A. De C.V. is recalling Next Advanced Antibacterial Hand Sanitizer because it contained methanol and had lower ethanol levels than labeled.

    Product
    NEXT ADVANCED ANTIBACTERIAL HAND SANITIZER (Ethyl Alcohol 70%), 8 FL OZ (236 ML) bottle, Made in Mexico, Distributed by: Genomma Lab USA Inc., Houston, TX 77027. UPC 6 50240 05357 3
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0452-2021·2020-11-25

    Cardinal Health Recalls Kangaroo Connect 500ml Bag Sets Due to Leakage

    Cardinal Health is recalling Kangaroo Connect 500ml Bag Sets because they may leak at the tube and spike connector interface.

    Product
    Kangaroo Connect 500ml Bag Set, Non-Sterile, Product Code 77500FD - Product Usage: single-use tubing sets used with pumps in the delivery of nutritional feeding product.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0457-2021·2020-11-25

    Stryker Recalls Osteosynthesis Compression Staple EasyClip Devices

    Stryker GmbH is recalling EasyClip and EasyClip Xpress staples due to potential nickel release above safety margins in pediatric patients under 20 kg.

    Product
    Osteosynthesis Compression Staple EasyClip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V737000·2020-11-25

    Audi recalls S5, A5, and RS5 for rear wiring defect

    Volkswagen Group (Audi) is recalling 2020-2021 S5, A5, and RS5 vehicles due to missing anti-abrasion protection on rear light wiring. In a crash, exposed wires may be damaged, potentially disabling door locks and hazard lights.

    Product
    AUDI — AUDI A5, RS 5, S5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0454-2021·2020-11-25

    MeritMedical Cultura Flex Swab Recall Due to Tip Breakage Risk

    Merit Medical Systems is recalling Cultura Flex Swabs because the flocked tip may break off during use, potentially causing soft tissue injury or treatment delays.

    Product
    MeritMedical Cultura Flex Swab, Sterile Flocked Collection Device, Ref C100F, Sterile, for the following unit count:1 unit - (01)00884450491102, 25 unit - (01)10884450491109, 100 unit - (01)20884450491106
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0449-2021·2020-11-25

    Thomas Scientific Recalls Wuxi Nest Patient Specimen Collection Tubes

    Thomas Scientific is recalling Wuxi Nest patient specimen collection tubes to replace units manufactured and distributed prior to Enforcement Discretion Approval.

    Product
    Wuxi Nest, model numbers 202115, 202117, 202017, 202018 - Product Usage: Patient specimen collection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21036·2020-11-25

    Santa Cruz Recalls 2020 Aluminum Bicycles Due to Frame Buckling Risk

    Santa Cruz Bicycles is recalling about 2,900 model year 2020 aluminum frames because thermal damage can cause them to bend or buckle, posing a fall hazard.

    Product
    Model Year 2020 Aluminum Santa Cruz and Juliana Bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·21034·2020-11-25

    RH Recalls Wine Barrel Chandeliers Due to Falling Hardware Hazard

    RH is recalling approximately 7,800 wine barrel chandeliers because hanging hardware can break, causing the fixture to fall. No injuries have been reported.

    Product
    Wine Barrel Chandeliers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V734000·2020-11-25

    Toyota RAV4 and Avalon Steering Column Airbag Failure Recall

    Certain 2020-2021 Toyota RAV4, RAV4 Hybrid, Avalon, and Avalon Hybrid vehicles may have damaged steering column breakaway pins that could reduce airbag performance in a crash. Toyota will replace the steering column at no cost.

    Product
    TOYOTA — TOYOTA AVALON, RAV4, AVALON HYBRID, RAV4 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V733000·2020-11-25

    Renegade Motorhomes Recalled for Gas Leak Risk in Cooking Stove

    Kibbi is recalling certain 2019-2021 Renegade motorhomes with Dometic cooking stoves due to a potential gas leak from an overtightened saddle valve bolt, which could increase fire risk. Dealers will install repair kits free of charge.

    Product
    RENEGADE — RENEGADE VERONA LE, VERONA, VALENCIA, CLASSIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0472-2021·2020-11-25

    Mako MICS Handpiece Recalled for Potential Bone Preparation Discrepancies

    Stryker is recalling Mako MICS Handpieces due to a characterization issue that may cause unsuccessful checkpoint verification or bone cuts differing from the preoperative plan.

    Product
    Mako Integrated Cutting System (MICS) Handpiece, Catalog Number 209063, Software Version#: THA 3.0 and later, PKA 3.0 and later, and TKA 1.0 - Product Usage: The MICS Handpiece is attached to the distal end of the robotic arm and is used to register the RIO (Mako robot) and to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0453-2021·2020-11-25

    Cardinal Health Recalls Kangaroo Connect 1000ml Bag Sets Due to Leak Risk

    Cardinal Health 200, LLC is recalling Kangaroo Connect 1000ml Bag Sets because the feeding spike sets may leak at the tube and spike connector interface.

    Product
    Kangaroo Connect 1000ml Bag Set, Non-Sterile, Product Code 77100FD - Product Usage: single-use tubing sets used with pumps in the delivery of nutritional feeding product.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0455-2021·2020-11-25

    Merit Medical Cultura Collection and Transport System recall due to swab tip breakage risk

    Merit Medical recalls its Cultura Collection and Transport System because the swab tip may break off during sample collection, potentially causing soft tissue injury.

    Product
    Merit Medical Cultura Collection and Transport System, Ref CFTS100, Single Use, IVD, for the following unit counts: 1 Unit - (01)00884450492123, 50 Units - (01)10884450492120, 200 units - (01)20884450492127
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0461-2021·2020-11-25

    Roche Recalls cobas infinity Software Due to Incorrect Validation

    Roche Diagnostics is recalling 40 cobas infinity central lab licenses because an erroneous QC status may cause incorrect validation of results.

    Product
    cobas infinity central lab/cobas infinity core license-The cobas infinity IT solutions application is intended to be used for the configuration and connectivity management of instruments and software systems Catalog Number: 07154003001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V736000·2020-11-25

    GM Recalls 2015-2016 Silverado and Sierra Trucks for Air Bag Defect

    General Motors is recalling 2015-2016 Chevrolet Silverado and GMC Sierra trucks because the roof-rail air bag inflator end cap may detach, posing an injury risk.

    Product
    CHEVROLET — CHEVROLET, GMC SILVERADO 1500, SIERRA 1500, SIERRA 2500, SIERRA 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0456-2021·2020-11-25

    Merit Medical Cultura Collection and Transport System Swab Tip Breakage Recall

    Merit Medical is recalling Cultura Collection and Transport Systems because the swab tip may break off during sample collection, potentially causing soft tissue injury.

    Product
    Merit Medical Cultura Collection and Transport System, 3 mL Viral Transport Medium, Ref: VCTS100, Single Use, IVD, for the following unit counts: 1 Unit - (01)00884450499917, 50 Units - (01)10884450499914, 200 units - (01)20884450499911
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21033·2020-11-25

    Herobility Eco Baby Spoons and Feeding Sets Recalled for Choking Hazard

    Herobility is recalling Eco Baby Spoons, Forks, and Feeding Sets because they can break into small pieces, posing a choking hazard. No injuries have been reported.

    Product
    Baby Spoons and Forks, Feeding Spoons and Placemat Feeding sets 4PCs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20V735000·2020-11-25

    Front Seat Bolts May Not Be Installed Properly in 2021 Chevrolet Tahoe

    Front seat attachment bolts may not have been properly installed on certain 2021 Chevrolet Tahoe, Suburban, and GMC Yukon models. If loose or missing, the seats could move during a crash, increasing injury risk.

    Product
    GMC — GMC, CHEVROLET YUKON, YUKON XL, TAHOE, SUBURBAN
    Category
    Vehicle
    Distribution
    Distributed nationwide