The Recall Desk

State

US Virgin Islands product recalls

73,366 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.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,366 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

19326–19350 of 73543

  • SevereCPSC·22210·2022-08-25

    Stand-up Paddleboard Paddles Recalled for Puncture and Laceration Risk

    Agit Global stand-up paddleboard paddles can suddenly break mid-shaft during use, exposing sharp edges. About 124,000 units sold nationwide from 2015–2020 pose a risk of serious puncture or laceration injuries.

    Product
    Paddles sold with stand-up paddleboards
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22211·2022-08-25

    Huffy Corporation Recalls Blue's Clues Ride-On Toys for Fall Hazard

    Huffy Corporation is recalling about 28,550 Blue's Clues Foot to Floor Ride-on Toys because the toy can tip forward when young children ride it, causing falls and injuries. The company has received 19 reports of children falling forward, resulting in 18 facial injuries.

    Product
    Blue's Clues Foot to Floor Ride-on Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22206·2022-08-25

    Steel Rolling Chassis for Utility Vehicles Recalled for Crash and Injury Hazards

    Navitas steel rolling chassis for utility vehicles are recalled because the throttle pedal can stick in the depressed position, creating crash and injury hazards. About 3,700 units distributed nationwide from June 2020 through April 2022 are affected.

    Product
    Steel rolling chassis for utility vehicles
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22207·2022-08-25

    Big Game Hunters Mud Kitchens Recalled for Excessive Lead Content

    About 190 Big Game Hunters Mud Kitchens are being recalled because the brass water tap contains lead levels that exceed federal safety limits. Lead is toxic if ingested by young children.

    Product
    Big Game Hunters Mud Kitchens
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22205·2022-08-25

    Kidoozie Activity Desk Toys Recalled for Entanglement and Entrapment Hazards

    Epoch Everlasting Play is recalling about 8,200 Kidoozie My First Activity Desk Toys due to entanglement and entrapment hazards. A protruding knob can become entangled with clothing, and the handle opening poses a jaw entrapment risk to children under 18 months.

    Product
    Kidoozie My First Activity Desk Toys
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22209·2022-08-25

    Trek Road Bicycles and Handlebar Stems Recalled for Handlebar Cracks

    Trek is recalling Model Year 2022 Speed Concept SLR bicycles, MY 2021-2022 Emonda SLR bicycles, and MY 2020-2021-2022 Bontrager Aeolus RSL VR-C aftermarket handlebar stems because carbon handlebars can crack, posing fall and crash hazards.

    Product
    Trek Model Year 2022 Speed Concept SLR and MY 2021-2022 Emonda SLR bicycles and MY 2020-2021-2022 aftermarket Bontrager Aeolus RSL VR-C handlebar/stems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·22208·2022-08-25

    IKEA Recalls METALLISK Espresso Makers Due to Burst and Burn Hazard

    IKEA is recalling METALLISK Espresso Makers with stainless-steel safety valves because the units can burst and expel hot contents, causing burn and scald injuries. About 2,100 units sold in the U.S. are affected.

    Product
    IKEA METALLISK Espresso Makers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·22V641000·2022-08-25

    2022 Rivian R1T and R1S Seat Belt Anchor Attachment Recall

    Rivian is recalling certain 2022 R1T and R1S vehicles because front seat belt anchors may be inadequately attached to the B-pillar, potentially preventing proper restraint during a crash.

    Product
    RIVIAN — RIVIAN R1T, R1S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V638000·2022-08-25

    2021 Jeep Gladiator rearview camera display failure from radio software error

    Certain 2021 Jeep Gladiator vehicles have a radio software error that may prevent the rearview camera image from displaying. This reduces rear visibility and increases the risk of backing collisions.

    Product
    JEEP — JEEP, RAM GLADIATOR, WRANGLER, 1500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·22767·2022-08-25

    Polaris Model Year 2022 PATRIOT BOOST Snowmobiles Recalled for Clutch Bolt Injury Hazard

    Polaris Industries is recalling about 2,300 Model Year 2022 PATRIOT BOOST RMK KHAOS and PATRIOT BOOST PRO RMK snowmobiles because the primary clutch bolt can break, causing clutch components to separate and create a projectile hazard.

    Product
    Polaris Snowmobiles, Model Year 2022 PATRIOT BOOST RMK KHAOS and PATRIOT BOOST PRO RMK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V637000·2022-08-24

    New Flyer Transit Buses Recalled for Steering Gear Fracture Risk

    New Flyer is recalling 2021-2022 transit buses because incorrectly assembled steering gears may fracture, potentially causing a loss of steering control.

    Product
    NEW FLYER — NEW FLYER XD40, XE40, XN40, XN35
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1512-2022·2022-08-24

    HeartWare HVAD System Batteries Recalled for Critical Electrical Faults

    HeartWare HVAD System Batteries are being recalled due to electrical faults that may prevent the battery from powering the device controller, accepting charges, or maintaining charge. Approximately 19,616 batteries distributed worldwide are affected.

    Product
    HeartWare Ventricular Assist Device (HVAD) System Batteries, Product Number 1650DE
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1532-2022·2022-08-24

    CURAD First Aid Kit Recalls Due to Improper Storage Temperature

    Family Dollar is recalling CURAD First Aid Kits (SKU 999037) that were improperly stored without temperature control from April 30 to June 10, 2022. The temperature exposure may have degraded medications or compromised medical devices within the kits.

    Product
    CURAD FIRST AID KIT, SKU 999037
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1524-2022·2022-08-24

    ARIES SARS-CoV-2 Assay may produce false negative diagnostic results

    Luminex Corporation recalled 257 units of the ARIES SARS-CoV-2 Assay (lot AB4042A) due to potential false negative results. The assay may fail to detect the ORF1ab gene, risking missed COVID-19 infections.

    Product
    ARIES SARS-CoV-2 Assay
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1345-2022·2022-08-24

    IV Trisodium Citrate Solution Recalled for Potential Cross-Contamination Risk

    Nephron Sterile Compounding Center is recalling 294 bags of Trisodium Citrate 0.5% Solution IV bags due to potential cross-contamination from manufacturing deviations. The affected lots were distributed nationwide.

    Product
    Trisodium Citrate 0.5% Solution, (0.5%/4L), contains Per Liter: Sodium 140 mmol/L, Chloride 86 mmol/L, Citrate 18 mmol/L, 4000 mL IV bag, packaged in 1 x 1 IV bag per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th Street Extension, West Columbia, SC 29172; NDC…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1543-2022·2022-08-24

    GS Saline Solution recalled due to improper temperature storage

    GS Saline Solution (12 fl oz) was not stored in temperature-controlled areas, risking contamination. The affected product was sold at Family Dollar stores nationwide from May 1–June 10, 2022.

    Product
    GS SALINE SOLUTION 12FL OZ, SKU 902274
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1546-2022·2022-08-24

    LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT Recalled Due to Improper Temperature Storage

    Family Dollar is recalling LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT that were stored without proper temperature control. Customers should discontinue use of product purchased between May 1 and June 10, 2022.

    Product
    LIFESTYLES ULTRA SENSITIVE CONDOMS 12CT, SKU 900265
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1545-2022·2022-08-24

    Simply Saline Nasal Mist Recalled for Improper Storage Conditions

    Simply Saline Nasal Mist 3.1 oz sold at Family Dollar stores has been recalled due to improper temperature storage between May and June 2022. Consumers should return the product to their local Family Dollar store.

    Product
    SIMPLY SALINE NASAL MIST 3.1 OZ, SKU 999801
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1517-2022·2022-08-24

    Sterile Surgical Pads and Wound Care Kits Recalled Due to Structural Failure

    ASO LLC is recalling 274,458 retail packages of three wound care products that fall apart during handling after removal from packaging, compromising their sterility and usability.

    Product
    (1) CVS Health Sterile Surgical Pads, Cushion Comfort, packaged 12 pads 5 in. x 9 in. per box, ASO Item No. 781083, SKU 894111 (2) CVS Health 30 Piece Wound Care Kit, For Large Size Wounds, ASO Item No. 781240, SKU 998842; and (3) equate First Aid Kit, 120 Items…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1526-2022·2022-08-24

    Pregnancy Test Units Recalled Due to Improper Temperature Storage

    Clearblue Smart Countdown pregnancy tests distributed to Family Dollar stores were not stored in temperature-controlled conditions. Consumers who purchased this product should return it for a refund or replacement.

    Product
    CLEARBLUE SMART COUNTDOWN PRGNCY TST 1CT, SKU-ID 900260
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-1344-2022·2022-08-24

    FDA Recalls Neostigmine Methylsulfate Injectable Due to Contamination Risk

    Nephron Sterile Compounding Center is recalling one lot of Neostigmine Methylsulfate Injection due to potential cross-contamination from product carryover during manufacturing. The recall affects 13,500 vials distributed nationwide.

    Product
    PF-Neostigmine Methylsulfate Injection, USP, 3 mg/3 mL (1 mg/mL), One 3 mL Unit-Dose Vial, packaged in 30 x 3 mL Sterile Unit-Dose Vials per carton, Rx Only, Nephron 503B Outsourcing Facility, 4500 12th Street Extension, West Columbia, SC 29172; NDC 69374-932-33
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1551-2022·2022-08-24

    Dressing Change Kit Recalled for Latex Mislabeling Risk

    Trinity Sterile is recalling Wolf Pak Premium Dressing Change Kits labeled as latex-free. The Non-Adherent Dressing component contains natural rubber latex, creating risk for patients with latex allergies.

    Product
    Wolf Pak Premium Dressing Change Kit with GuardVA and Statlok Cs/30 Ref: DC5090LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1549-2022·2022-08-24

    Medical Dressing Kit Recalled for Mislabeled Latex Content

    Wolf-Pak Premium Dressing Kits labeled latex-free are being recalled because a component contains natural rubber latex, posing a risk to people with latex allergies.

    Product
    Wolf-Pak Premium Dressing Kit with GuardVA Cs/30 Ref: DC5030LF
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1555-2022·2022-08-24

    BD PhaSeal Y-Site Connector recalled for mislabeled expiration dates

    Becton Dickinson recalls 9,340 units of BD PhaSeal Y-Site Connectors (Catalog 515304) due to incorrect expiration dates printed on product labels that extend beyond the actual product expiration.

    Product
    BD PhaSealTM Y-Site Connector (C80)- airtight and leak-proof Closed System Drug Transfer Device (CSTD) that mechanically prohibits the transfer of environmental contaminants into the system and the escape of drug or vapor concentrations outside the system. Catalog Number…
    Category
    Medical Device
    Distribution
    Distributed nationwide