The Recall Desk

State

US Virgin Islands product recalls

73,096 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
30
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 30 (17%) are Severe.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,096 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

10776–10800 of 73273

  • HighFDA (Drugs)·D-0560-2024·2024-06-26

    White Petrolatum Jelly Mislabeled With Undisclosed Lavender and Chamomile

    Consumer Product Partners is recalling Pure Petroleum white petrolatum products sold at Rite Aid, Kroger, Harris Teeter, and CVS nationwide because the products labeled as pure white petrolatum actually contain undisclosed lavender and chamomile.

    Product
    PURE PETROLEUM — PURE PETROLEUM (WHITE PETROLATUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2149-2024·2024-06-26

    Ethicon MONOCRYL Plus Sutures Recalled for Packaging Defect

    Ethicon recalled 287,892 MONOCRYL Plus Antibacterial Sutures worldwide due to a packaging machine defect that created holes in primary packaging, potentially compromising sterility and risking infection.

    Product
    MONOCRYL Plus Antibacterial (poliglecaprone 25) Suture - Intended for use in general soft tissue approximation and/or ligation where an absorbable material is indicated. PRODUCT CODE: MCP266H13 MCP3200H16 MCP3212H16 MCP3213H16 MCP340H13 MCP345H13 MCP416H14 MCP417H14 M
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2144-2024·2024-06-26

    VICRYL Sutures recalled due to packaging defect compromising sterility

    Ethicon recalls 341,532 units of VICRYL surgical sutures worldwide due to holes in primary packaging that compromise sterility and could result in infection.

    Product
    VICRYL (polyglactin 910) Suture - Indicated for use in general soft tissue approximation and/or ligation, including use in ophthalmic surgery, but not for use in cardiovascular and neurological tissues. PRODUCT CODE: J214H J218H J258H J268H J269H J327H J344H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2148-2024·2024-06-26

    MONOCRYL Surgical Sutures Recalled for Packaging Sterility Defect

    Ethicon recalls 306,000 MONOCRYL surgical sutures worldwide due to holes in primary packaging from a manufacturing defect that compromises sterility and could result in infection.

    Product
    MONOCRYL (poliglecaprone 25) Suture - Intended for use in general soft tissue approximation and/or ligation where an absorbable material is indicated PRODUCT CODE: Y315H Y345H Y359H Y398H Y416H Y417H Y426H Y427H Y935H Y936H Y945H
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2147-2024·2024-06-26

    PDS Plus Antibacterial Surgical Sutures Recalled for Compromised Sterility

    Ethicon recalls PDS Plus Antibacterial sutures due to packaging defects that compromised sterility. The affected units may cause infection if used in surgery.

    Product
    PDS Plus Antibacterial (polydioxanone) Suture - Intended for use in general soft tissue approximation, including use in paediatric cardiovascular tissue, in microsurgery and in ophthalmic surgery. These sutures are particularly useful where the combination of an absorbable suture
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2146-2024·2024-06-26

    PDS II Polydioxanone Sutures Recalled Due to Compromised Sterility

    Ethicon is recalling 56,952 units of PDS II polydioxanone sutures distributed worldwide because a packaging defect resulted in compromised sterility, which could lead to infection. No illnesses have been reported.

    Product
    PDS II (polydioxanone) Suture - Intended for use in general soft tissue approximation, including use in paediatric cardiovascular tissue, in microsurgery and in ophthalmic surgery. These sutures are particularly useful where the combination of an absorbable suture and extended wo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2162-2024·2024-06-26

    Xstar Safety Slit Knife Recalled for Incorrect Blade Configuration

    Beaver Visitec International is recalling 126 Xstar Safety Slit Knives with incorrect blade configuration. The recalled knives have the bevel oriented to the back instead of the front.

    Product
    Xstar Safety Slit Knife, 2.75 mm 45¿ Bevel Up, Model Number 378227, a component of CustomEye Kits, Numbers 584562, 5800109
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0556-2024·2024-06-26

    Drug Recall: Eptifibatide Injection Due to Failed Degradation Specifications

    Eugia US LLC is recalling 15,500 vials of Eptifibatide injection nationwide due to failed impurities and degradation specifications. The defect involves a related substance identified as Eptifibatide dimer.

    Product
    EPTIFIBATIDE — EPTIFIBATIDE (EPTIFIBATIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V475000·2024-06-25

    SEA Electric Recalls 174 Vehicles Due to Battery Software Defect

    SEA Electric is recalling 174 vehicles because a software defect may cause the high-voltage battery to shut down, resulting in a loss of drive power.

    Product
    SEA ELECTRIC — SEA ELECTRIC FORD F59, 5E, ISUZU NRR, HINO 195
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24281·2024-06-25

    MGA Entertainment Recalls Miniverse Make It Mini Sets with Liquid Resins

    MGA Entertainment recalls about 21 million Miniverse Make It Mini Sets with unused liquid resins due to risk of skin, eye, and respiratory irritation. The recalled sets contain acrylates in amounts prohibited in children's products.

    Product
    Miniverse Make It Mini Sets with Liquid Resins
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·24E052000·2024-06-25

    SEA Electric Recalls Electric Vehicle Battery Management Software

    SEA Electric is recalling certain electric vehicles because a software defect in the battery management system can cause a loss of drive power, increasing crash risk.

    Product
    ELECTRICAL SYSTEM:PROPULSION SYSTEM:TRACTION BATTERY:MANAGEMENT SYSTEM/ENERGY CONTROL MODULE (BMS/BECM):SOFTWARE recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V471000·2024-06-24

    Oshkosh Defense NGDV ICE Recalled for Air Bag Deployment Risk

    Oshkosh is recalling 2025 Defense NGDV ICE vehicles because deformed wiring harness terminals may prevent air bags from deploying as intended.

    Product
    OSHKOSH — OSHKOSH DEFENSE NGDV ICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V451000·2024-06-24

    Jaguar F-Pace oil filter housings can crack and leak oil

    Jaguar is recalling certain 2021-2024 F-Pace vehicles because the oil filter housing can crack and leak oil into the engine compartment. 150 units are affected.

    Product
    JAGUAR — JAGUAR F-PACE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V467000·2024-06-21

    Isuzu Recalls 2025 FTR Trucks Due to Tie Rod Assembly Defect

    Isuzu is recalling 2025 FTR vehicles because incorrectly heat-treated ball studs in the tie rod assemblies may break, potentially causing loss of steering control.

    Product
    ISUZU — ISUZU FTR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V470000·2024-06-21

    Nissan Recalls INFINITI Vehicles for Driveshaft Fatigue and Breakage Risk

    Nissan is recalling specific INFINITI models because the driveshaft can fatigue and break, potentially causing loss of drive power or vehicle roll-away.

    Product
    INFINITI — INFINITI Q70, Q50, Q70L, Q70 HYBRID
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V468000·2024-06-21

    REV Ambulance Recalls 2019-2024 Vehicles Due to Outrigger Bolt Defect

    REV Ambulance is recalling 160 emergency vehicles because improperly tightened outrigger bolts may cause the module box to detach or the outrigger to fail.

    Product
    REV AMBULANCE — REV AMBULANCE TYPE IX, TYPE I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24E050000·2024-06-21

    AROW Recalls MV210 Emergency Exit Windows Due to Latch Failure Risk

    AROW Global Corp is recalling MV210 emergency exit windows because the latch can fail during a crash, potentially allowing the window to open and increasing injury risk.

    Product
    STRUCTURE:EMERGENCY:ESCAPE/EGRESS/EXIT:LATCHING/RELEASE SYSTEM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24E051000·2024-06-20

    Hendrickson Lift Axle Suspension Recall for Tie Rod Assembly Defect

    Hendrickson is recalling 461 steerable lift axle suspension assemblies because the tie rod ball stud may fail, creating a road hazard.

    Product
    STEERING:LINKAGES:TIE ROD ASSEMBLY recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V462000·2024-06-20

    International truck tie rod ball studs were incorrectly heat treated

    Navistar is recalling certain 2025 International HV, LT, MV and RH trucks because tie rod ball studs may have been incorrectly heat-treated and can break. 116 units affected.

    Product
    INTERNATIONAL — INTERNATIONAL RH, HV, MV, LT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·24272·2024-06-20

    JoyJolt Declan Glass Coffee Mugs Recalled for Burn and Laceration Hazards

    MM Products is recalling about 580,000 JoyJolt Declan single-wall glass coffee mugs because they can break and crack when filled with hot liquids, posing burn and laceration hazards. The mugs were sold online from September 2019 through May 2022.

    Product
    JoyJolt Drinkware Declan Single-Wall Glass Coffee Mugs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·24273·2024-06-20

    Frontgate Newport Chaise Lounge Chairs Recalled for Finger Crushing and Amputation

    Cinmar recalls approximately 70,000 Frontgate Resort Collection Newport aluminum and teak chaise lounge chairs because the adjustable backrest can descend with force while seated, causing finger crushing and amputation injuries.

    Product
    Frontgate Resort Collection Newport Aluminum and Teak Chaises
    Category
    Consumer Product
    Distribution
    Distributed nationwide