The Recall Desk

State

US Virgin Islands product recalls

73,106 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 73,106 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

13251–13275 of 73283

  • HighFDA (Devices)·Z-0525-2024·2023-12-20

    Medline Sterile PVP Solution Recalled Due to Non-Sterile Contents

    Medline Industries is recalling 8,250 units of sterile PVP solution distributed nationwide because the contents are non-sterile despite being labeled as sterile.

    Product
    STERILE PVP SOLUTION, REF DYNDA1907
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0552-2024·2023-12-20

    GE Definium Tempo X-Ray System Bolts May Loosen and Fall

    Incorrect bolt torque on GE Definium Tempo X-ray systems may cause the overhead tube suspension assembly to fall. No injuries have been reported, but GE recommends immediate inspection of affected systems.

    Product
    The System is designed as a modular system with components that include an Overhead Tube Suspension with tube/collimator, wallstand, Table, X-ray generator, and cleared wireless digital detectors. The list of detectors verified and validated for use with the Discovery XR656 HD…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0557-2024·2023-12-20

    Olympus tracheal intubation fiberscope recalled due to suction flow specification issue

    Olympus tracheal intubation fiberscopes are being recalled because the manufacturer lacks adequate data confirming the suction flow rate meets device specifications. No injuries have been reported.

    Product
    TRACHEAL INTUBATION FIBERSCOPE OLYMPUS LF-GP, Model Number: LF-GP
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0518-2024·2023-12-20

    Iconix Knotless 1.4mm Anchor recalled due to inserter failure risk

    Riverpoint Medical is recalling Iconix Knotless 1.4mm surgical anchors because the inserter can fail or bend when used in hard bone, potentially damaging sutures during insertion or use.

    Product
    Iconix Knotless 1.4mm Anchor with XBraid S (Blue/Black) REF 3911-714-520 Iconix Knotless 1.4mm Anchor with XBraid S (Black/White) REF 3911-714-521 The Iconix Knotless anchors are intended to be used for soft-tissue to bone fixation in the foot, ankle, knee, hip, hand…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·23V866000·2023-12-20

    2023 Nova Bus LFS Suspension Hardware May Separate

    Nova Bus is recalling 2023 LFS buses because the front air spring suspension hardware may separate from its attachment plate, potentially causing sudden loss of suspension and vehicle control.

    Product
    NOVA BUS — NOVA BUS LFS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0547-2024·2023-12-20

    Laboratory Diagnostic System Software Malfunction Causes System Freezes and Delays

    Ortho-Clinical Diagnostics recalls 216 VITROS XT 7600 laboratory systems running Software Version 3.8.0 due to software issues causing screen freezes and unresponsiveness. The defects delay test result reporting and could postpone patient treatment.

    Product
    VITROS XT 7600 Integrated System Product Code 6844461 Running Software Version 3.8.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0546-2024·2023-12-20

    Chemistry System Software Malfunction Causes Freezes and Result Reporting Delays

    Ortho-Clinical Diagnostics is recalling VITROS XT 3400 Chemistry Systems due to software issues causing screen freezes and system unresponsiveness. The problems can delay reporting of patient test results, including critical or STAT assays.

    Product
    VITROS XT 3400 Chemistry System Product Code 6844458 Running Software Version 3.8.0
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0530-2024·2023-12-20

    Non-sterile Betadine solution labeled and distributed as sterile

    Medline Industries is recalling 1,800 units of Sterile Betadine (Ref DYNDA1998) because the foil sachet contents are non-sterile, despite labeling that claims sterility. The recall affects units nationwide in eight states.

    Product
    STERILE BETADINE, REF DYNDA1998
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0521-2024·2023-12-20

    Cardinal Health Stool Transportation System Recalled for Vial Leakage

    Meridian Bioscience is recalling the Cardinal Health Clean Stool Transportation System due to a manufacturing defect that may cause Para-Pak vials to leak. Affected product: 38 cases with Lot Number 510020Q, distributed nationwide and to Italy.

    Product
    Cardinal Health Clean Stool Transportation System-For the collection, transportation, preservation, and examination of stool specimens containing intestinal parasites Catalog Number: CHB900312
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0509-2024·2023-12-20

    Spectranetics Turbo-Elite Atherectomy Catheters recalled due to labeling mismatch

    Spectranetics Corporation is recalling 1,239 Turbo-Elite Laser Atherectomy Catheters due to incorrect labeling where the exterior product box label does not match the internal pouch label.

    Product
    Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 RX REF 420-159 Spectranetics Turbo-Elite Laser Atherectomy Catheter 2.0 OTW REF 420-006 Spectranetics Turbo-Elite Laser Atherectomy Catheter 1.4 RX REF 414-159 Spectranetics Turbo-Elite Laser Atherectomy Catheter…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0150-2024·2023-12-20

    Liothyronine Sodium tablets recalled due to failed impurity and degradation specifications

    Sun Pharmaceutical is recalling 96,192 bottles of Liothyronine Sodium Tablets nationwide due to failed quality specifications for impurities and degradation. The affected lots were distributed in 100-count bottles.

    Product
    LIOTHYRONINE SODIUM — LIOTHYRONINE SODIUM (LIOTHYRONINE SODIUM)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0556-2024·2023-12-20

    Medical Device Instructions Update Recall for Navik 3D Mapping System

    APN Health LLC is recalling the Navik 3D v2 3D Mapping System to update the product instructions for use. The firm initiated this voluntary recall.

    Product
    Navik 3D v2, REF NAVIK3D, 3D Mapping System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V862000·2023-12-19

    2022-2023 Tesla Model S and X Door Latch Safety Defect Recall

    Certain 2022-2023 Tesla Model S and X vehicles may have cabin doors that unlock during a crash due to a door latch defect. Tesla is providing a free over-the-air software update to fix the issue.

    Product
    TESLA — TESLA MODEL S, MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V861000·2023-12-19

    Van Hool Recalls 2024 CX45 Vehicles Due to Seat Belt Screw Defect

    Van Hool is recalling 64 2024 CX45 vehicles because a seat belt assembly screw may break. This defect could prevent the seat belt from properly restraining occupants during a crash.

    Product
    VAN HOOL — VAN HOOL CX45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V859000·2023-12-19

    Doosan Portable Generator Trailers Recalled for Brake Wiring Defect

    Doosan is recalling 2019-2023 Portable Generator Trailers because the electric brake harness was incorrectly wired, causing brakes to fail when the battery switch is off.

    Product
    DOOSAN PORTABLE POWER — DOOSAN PORTABLE POWER MOBILE GENERATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V860000·2023-12-19

    Airstream Basecamp Travel Trailers Recalled for Failing Spare Tire Bracket

    The spare tire carrier bracket on certain 2012-2023 Airstream Basecamp travel trailers may experience metal fatigue and break, causing the spare tire to detach and become a road hazard. Airstream is providing free replacement and reinforcement of the bracket.

    Product
    AIRSTREAM — AIRSTREAM BASECAMP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V858000·2023-12-18

    Fuel pump failure recall for 2013-2023 Honda and Acura vehicles

    Honda is recalling certain 2013-2023 Honda Accord, Civic, CR-V, HR-V, Odyssey, Pilot, Ridgeline and Acura ILX, MDX, RDX, RLX, TLX vehicles because the fuel pump inside the fuel tank may fail, potentially causing engine stall while driving and increasing crash risk.

    Product
    HONDA — HONDA, ACURA ACCORD HYBRID, CIVIC, PILOT, RDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23E095000·2023-12-18

    Hendrickson Lift Axle Recall Due to Steering Knuckle Assembly Defect

    Hendrickson is recalling certain COMPOSILITE EXS20 and SC20 Lift Axles because bearing journals may not be fully seated, increasing the risk of a crash.

    Product
    STEERING:LINKAGES:KNUCKLE:SPINDLE:ARM recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V857000·2023-12-18

    2024 PJ Trailers Recalled: Defective Tires Cause Pressure Loss

    PJ Trailers is recalling 2024 model trailers due to defective tires that may experience sidewall separation and pressure loss. Dealers will replace affected tires free of charge.

    Product
    PJ TRAILERS — PJ TRAILERS DT, DG, CE, C8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·23V856000·2023-12-17

    Can-Am Spyder F3 Motorcycle Rearview Mirror Lens Dislodgment Recall

    Bombardier Recreational Products is recalling 2023 Can-Am Spyder F3 and F3-S motorcycles because the rearview mirror lens may dislodge from the housing, reducing driver visibility and increasing crash risk. Dealers will install new mirror assemblies free of charge.

    Product
    CAN-AM — CAN-AM SPYDER F3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V850000·2023-12-15

    Coachmen Concord Motorhomes Recalled for Air Suspension Line Defect

    Forest River is recalling 2023-2024 Coachmen Concord motorhomes because an air suspension line may be installed near the exhaust, risking sudden suspension loss and vehicle control issues.

    Product
    COACHMEN — COACHMEN CONCORD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V854000·2023-12-15

    Mercedes-Benz Recalls Vehicles for Potential Front Roof Panel Detachment

    Mercedes-Benz is recalling 2014-2020 models because the front roof panel may detach, creating a road hazard and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES-MAYBACH redundant S550E, C 350 E, GLA 250, S 560 4MATIC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·23V851000·2023-12-15

    Mercedes-Benz Recalls 2022-2023 AMG G63 Due to Rear Axle Cracks

    Mercedes-Benz is recalling 2022-2023 AMG G63 vehicles because the rear axle differential housing may crack, potentially causing oil leaks or axle failure.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG G63
    Category
    Vehicle
    Distribution
    Distributed nationwide