The Recall Desk

State

US Virgin Islands product recalls

73,104 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.

Which agencies issued them

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,104 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

11851–11875 of 73281

  • ModerateFDA (Devices)·Z-1413-2024·2024-04-10

    Exactech Equinoxe Shoulder Implants Recalled for Nonconforming Packaging

    Exactech is recalling 12,643 units of Equinoxe CAGE GLENOID shoulder implants because packaging lacks a required oxygen barrier layer. Units were vacuum-sealed without the proper Ethylene Vinyl Alcohol (EVOH) barrier.

    Product
    Exactech Equinoxe CAGE GLENOID, CEMENTED, beta curvature, Mates with: a) 47, 50, 53 head, Medium, Item Number 314-13-13, b) 47, 50, 53 head, Large, Item Number 314-13-14, c) 47, 50, 53 head, Extra Large, Item Number 314-13-15; Shoulder Arthroplasty
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1400-2024·2024-04-10

    Hill-Rom PRO+ Pressure Relief Mattress Service Correction Reassessment

    Baxter Healthcare is reassessing 232 Hill-Rom PRO+ pressure relief mattresses due to identified inconsistencies in service records from a previous correction. These mattresses must be verified to confirm corrections were properly applied.

    Product
    Hill-Rom PRO+ 36" MRS Surface, REF P7924A03, The pro+ mattress is intended for patient support and for the prevention and/or treatment of pressure injuries.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1409-2024·2024-04-10

    Exactech Equinoxe Shoulder Arthroplasty Components Recalled for Defective Packaging

    Exactech recalls 39 UHMWPE shoulder arthroplasty components due to nonconforming vacuum packaging that lacks the required oxygen barrier layer.

    Product
    Exactech Equinoxe GLENOID,POSTERIOR AUGMENT, PEGGED, 12o, RIGHT, FOR CEMENTED USE ONLY, Mates with: a) 38, 41, 44, 47 head, Small, Item Number 314-04-32, b) 41, 44, 47, 50 head, Medium, Item Number 314-04-33, c) 44, 47, 50, 53 head, Large, Item Number 314-04-34, d)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1421-2024·2024-04-10

    Exactech Equinoxe Shoulder Arthroplasty Liner Recalled for Nonconforming Packaging

    Exactech recalls 447 units of Equinoxe Constrained Humeral Liner due to nonconforming packaging lacking required oxygen barrier layer (EVOH). Affected units were distributed nationwide and internationally.

    Product
    Exactech Equinoxe Constrained Humeral Liner: Item Numbers: a) 320-40-10, b) 320-40-13, Shoulder Arthroplasty
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1404-2024·2024-04-10

    Exactech Shoulder Implant Components Recalled for Nonconforming Oxygen Barrier Packaging

    Exactech Inc. is recalling 6,678 shoulder glenoid implant components because they were packaged in vacuum bags lacking the required oxygen barrier layer made of Ethylene Vinyl Alcohol (EVOH).

    Product
    Exactech Equinoxe GLENOID,KEELED, CEMENTED, mates with 47, 50, 53 head, beta curvature, Sizes: a) Small, Item Number 314-02-02, b) Medium, Item Number 314-02-03, c) Large, Item Number 314-02-04, Shoulder Arthroplasty
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0433-2024·2024-04-10

    Cyclophosphamide Injection Recalled for Package Insert Concentration Labeling Error

    X-Gen Pharmaceuticals is recalling 1,283 vials of Cyclophosphamide for Injection due to a Package Insert error that lists concentration as '20 mg per vial' instead of '20 mg per mL'. No illnesses have been reported.

    Product
    Cyclophosphamide for Injection, USP, 500mg/vial, Lyophilized, Cytotoxic Agent, Single Dose Vial for Intravenous Use, Rx Only, Manufactured for: XGen Pharmaceuticals DJB, Inc. Big Flats, NY 14814, NDC # 39822-0250-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0434-2024·2024-04-10

    Cyclophosphamide Injection Recalled for Package Insert Concentration Labeling Error

    X-Gen Pharmaceuticals recalls Cyclophosphamide for Injection due to a labeling error in the Package Insert. Section 2.3 incorrectly lists the concentration as '20 mg per vial' instead of the correct '20 mg per mL'.

    Product
    Cyclophosphamide for Injection, USP, 1g/vial, Lyophilized, Single Dose Vial, Discard unused solution, Cytotoxic Agent, After Reconstitution: For direct intravenous injection or must be further diluted before intravenous infusion, Rx Only, Manufactured for: XGen Pharmaceuticals…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V253000·2024-04-05

    Forest River Recalls Transit Buses Due to Unsecured Brake Lines

    Forest River Bus is recalling specific 2018-2024 transit bus models because unsecured brake lines may be damaged by the frame rail, increasing crash risk.

    Product
    STARCRAFT BUS — STARCRAFT BUS, ELDORADO, ELKHART SENATOR II, CANDIDATE II, ADVANTAGE, ALLSTAR MVP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V080000·2024-04-05

    Autocar Recalls 2023 Xpeditor and Xspotter Vehicles for Steering Defect

    Autocar is recalling 2023 Xpeditor and Xspotter vehicles because steering gears may have fewer recirculating balls than required, risking loss of steering control.

    Product
    AUTOCAR — AUTOCAR XSPOTTER, XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V254000·2024-04-05

    2024 Coachmen Catalina and Aurora Travel Trailers: Electrical Fire Risk

    Forest River is recalling certain 2024 Coachmen Catalina and Aurora Travel Trailers due to improper routing of the distribution panel wire. The unprotected wire increases the risk of fire.

    Product
    FOREST RIVER — FOREST RIVER, COACHMEN AURORA, CATALINA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·24V255000·2024-04-05

    Aston Martin DBX electrical cable defect may cause engine stall

    Aston Martin is recalling 2021-2024 DBX vehicles due to loose electrical cables in the battery fuse box, which may cause engine stall, loss of headlights, or loss of power steering, increasing crash risk.

    Product
    ASTON MARTIN — ASTON MARTIN DBX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24189·2024-04-05

    Procter & Gamble Recalls 8.2 Million Defective Laundry Detergent Packet Bags

    Procter & Gamble is recalling about 8.2 million bags of Tide, Gain, Ace, and Ariel laundry detergent packets because the outer packaging can split open near the zipper, risking serious injury, ingestion, or skin or eye injuries—especially to children.

    Product
    Tide Pods, Gain Flings, Ace Pods and Ariel Pods liquid laundry detergent packets packaged in flexible film bags. This recall announcement applies only to bags distributed in the United States.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·24180·2024-04-04

    C2 Crank Cocking Aids for Excalibur Crossbows Recalled for Impact Injury and Laceration Hazards

    Excalibur Crossbow is recalling about 15,000 C2 Crank cocking aids because the plastic cocking hooks can break during use and become flying projectiles, causing impact injuries and lacerations. One consumer reportedly suffered a permanent eye injury.

    Product
    C2 Crank Cocking Aid for Crossbows
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalCPSC·24179·2024-04-04

    Essential Medical Supply Reannounces Adult Bed Rails Recall; Entrapment and Asphyxia

    Essential Medical Supply is reannouncing a recall of approximately 272,000 Endurance® Hand Bed Rails due to entrapment and asphyxiation hazards. Two additional deaths have been reported since the original 2021 recall.

    Product
    Endurance® Hand Bed Rails
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·24181·2024-04-04

    BLACK+DECKER Garment Steamers Recalled Nationwide for Burn Hazard

    Empower Brands is recalling approximately 1.6 million BLACK+DECKER Model HGS011 Easy Garment Steamers because they can expel, spray, or leak hot water during use, causing burn injuries. Consumers should stop using the steamers immediately and contact the manufacturer for a full refund.

    Product
    BLACK+DECKER Model HGS011 Easy Garment Steamers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·24V252000·2024-04-04

    Terex Advance Recalls 2023 Commander Vehicles for Steering Defect

    Terex Advance is recalling 2023 Commander vehicles because steering components may not be installed correctly, increasing the risk of a crash.

    Product
    TEREX ADVANCE — TEREX ADVANCE COMMANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·24184·2024-04-04

    Zazaba International Recalls Grão de Gente Baby Nests for Suffocation and Fall Hazards

    Zazaba International is recalling about 430 Grão de Gente baby nests sold online from March 2023 through August 2023 due to suffocation risk and fall and entrapment hazards that violate federal infant sleep product safety standards.

    Product
    Grão de Gente Baby Nests
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24178·2024-04-04

    Walmart Recalls Mainstays Electric Mini Choppers for Laceration Hazard

    Walmart is recalling about 51,750 Mainstays Electric Mini Choppers because the blade can operate unexpectedly during assembly or when not enclosed, causing cuts. Five lacerations have been reported, two requiring medical attention.

    Product
    Mainstays Electric Mini Choppers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·24185·2024-04-04

    Zazaba International Recalls Grão de Gente Crib Bumper Bedding Sets for Suffocation Risk

    Zazaba International is recalling about 795 Grão de Gente padded crib bumper bedding sets sold online between March and August 2023 due to suffocation hazard. Infants can suffocate if they roll into the bumper, which violates the federal Safe Sleep for Babies Act of 2021.

    Product
    Grão de Gente Crib Bumper Bedding Sets
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24183·2024-04-04

    Children's Two-Piece Pajamas and Lounge Dresses Flammability Violation Recall

    Koala Tree Enterprises (DBA Lovey & Grink) is recalling approximately 23,720 children's two-piece pajamas and lounge dresses because they violate federal flammability regulations for children's sleepwear and pose a risk of burn injuries.

    Product
    Children's Two-Piece Pajamas and Lounge Dresses
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • ModerateCPSC·24182·2024-04-04

    Thule RideAlong Rear-Mounted Child Bike Seats Recalled for Chemical Hazard

    Thule is recalling about 8,640 RideAlong rear-mounted child bike seats because the harness padding can contain DecaBDE, a flame retardant, in excess of regulatory limits. DecaBDE can be toxic if ingested or if it contacts skin or eyes.

    Product
    Thule RideAlong rear-mounted Child Bike Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1326-2024·2024-04-03

    Catheter Extension Recalled by Fresenius Due to Chemical Leachables

    Fresenius is recalling 479,978 stay-safe Luer Lock Catheter Extensions due to chemical leachables in the tubing. Healthcare providers should contact the manufacturer for replacement information.

    Product
    stay-safe /Luer Lock Catheter Ext. 18 in
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1286-2024·2024-04-03

    Nimbus II Infusion Pump Systems Recalled for Multiple Potential Device Failures

    InfuTronix is recalling 52,328 Nimbus II Infusion Pump Systems due to potential failure modes including battery failure, system errors, drug product leakage, flow rate issues, and housing damage. The devices will no longer be available or supported after June 20, 2024.

    Product
    Nimbus II Infusion System; Nimbus II PainPRO IT1053; Nimbus II Flex IT1062; Nimbus II Plus IT1078; Nimbus II EpiD IT1124; Nimbus II EMS IT1063; Ambulatory Infusion Pump and components
    Category
    Medical Device
    Distribution
    Distributed nationwide