The Recall Desk

State

US Virgin Islands product recalls

73,827 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 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56926–56950 of 74005

  • ModerateFDA (Devices)·Z-2687-2014·2014-10-01

    Beckman Coulter Recalls Sample Probe Cables for Immunoassay Systems

    Beckman Coulter is recalling sample probe cables for UniCel immunoassay systems because nonconforming units may cause delays in reporting test results.

    Product
    UniCel 600/800 Access Immunoassay Systems are in vitro diagnostic devices used for the quantitative, semi-quantitative, or qualitative determination of various analytes concentrations found in human body fluids. The cables and kits are used in UniCel DxI 600, 800 instruments…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1605-2014·2014-10-01

    Qualitest Recalls Subpotent Methylprednisolone Tablets Due to Stability Issues

    Qualitest Pharmaceuticals is recalling specific lots of Methylprednisolone 4 mg tablets because they may be subpotent due to a 6-month stability time point issue.

    Product
    METHYLPREDNISOLONE — METHYLPREDNISOLONE (METHYLPREDNISOLONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2708-2014·2014-10-01

    Dako Autostainer Link 48 Software Recall for Reagent Handling Issues

    Dako is recalling software for the Autostainer Link 48 because an upgrade may cause premature reagent rejection or inadequate aspiration if specific maintenance conditions are met.

    Product
    Dako Autostainer Link 48 with software version Dako Link 4.0.3, Model No. AS480 Product Usage: For in vitro diagnostic use. The Dako Autostainer Link 48 is an automated slide processing system compatible with reagents for the staining of paraffin-embedded and frozen tissue…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2692-2014·2014-10-01

    Horiba Medical Recalls ABX PENTRA Magnesium RTU Reagent for Stability Update

    Horiba Medical is recalling ABX PENTRA Magnesium RTU Reagent to update on-board stability claims from 7 days to 1 day.

    Product
    ABX PENTRA Magnesium RTU Reagent, Part No. A11A01646 Product Usage: ABX PENTRA Magnesium RTU reagent with associated calibrators and controls are for quantitative in vitro diagnostic determination of magnesium in human serum and plasma based on a photometric test using…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2680-2014·2014-10-01

    Siemens Ysio Systems Recalled for Potential Image Artifacts

    Siemens is recalling 62 Ysio Systems due to a software error that may cause line artifacts in images, potentially requiring examinations to be repeated.

    Product
    The Ysio Systems with software version VC10 The Ysio enables radiographic and tomographic exposures of the whole Body including: skull, chest, abdomen, and extremities and may be used on pediatric, adult and bariatric patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1608-2014·2014-10-01

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Pharmaceuticals is recalling 160,800 Daytrana patches because the adhesive release liner may be difficult to remove.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2672-2014·2014-10-01

    Vidacare EZ-IO Needle Set Recalled for Specification Failures

    Vidacare Corporation is voluntarily recalling 172 units of EZ-IO 45mm Needle Sets because they do not meet specifications.

    Product
    EZ-IO 45mm (40kg & up) Needle Set, part number 9079-VC-005; lot code 3606455
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2673-2014·2014-10-01

    Becton Dickinson Recalls BD PosiFlush SF Saline Flush Syringes Due to Open Seals

    Becton Dickinson is recalling 3,088,320 units of BD PosiFlush SF Saline Flush Syringes because some units were found with open seals.

    Product
    BD PosiFlush SF Saline Flush Syringe 0.9 Sodium Chloride Injection, USP 10 mL REF 306553. Intended to be used only for the flushing of indwelling vascular access devices.10 mL BD PosiFlush Normal Saline Flush Syringes are generally compatible for use with syringe pumps.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-2513-2014·2014-10-01

    Frito-Lay Recalls Oven Baked Lay's BBQ Crisps Due to Packaging Error

    Frito-Lay is recalling Oven Baked Lay's BBQ flavor crisps because a packaging error added a 'GF' symbol to the packages.

    Product
    Oven Baked Lay's BBQ flavor crisps in 1 1/8 oz package, UPC 2840007189
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2679-2014·2014-10-01

    Instratek Recalls Mini Screw Sets with Faded Markings

    Instratek is recalling 96 Mini Screw Sets and gauges due to faded and incorrect markings on instruments.

    Product
    Mini Cannulated Titanium Headed and Headless Screw Set and 2.5, 3.0, and 4.0 mm countersink/depth gauges in the Mini Screw Set/System
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1607-2014·2014-10-01

    Alvogen Recalls Oxycodone and Acetaminophen Tablets Due to Uniformity Failure

    Alvogen, Inc. is recalling 8,964 bottles of Oxycodone and Acetaminophen Tablets USP 10 mg/325 mg because the lot failed uniformity of dosage units specifications for the oxycodone component.

    Product
    Oxycodone and Acetaminophen Tablets USP 10 mg/325 mg 100 count bottles Rx Only. Manufactured by Norwich Pharmaceuticals Inc., Norwich, NY 13185 USA; Distributed by Alvogen Inc, Pine Brook NJ 07058 USA.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2688-2014·2014-10-01

    Smith & Nephew Recalls RENASYS EZ Negative Pressure Wound Therapy Systems

    Smith & Nephew is recalling RENASYS EZ Negative Pressure Wound Therapy Systems because modifications were made without required FDA notifications.

    Product
    RENASYS EZ Negative Pressure Wound Therapy (NPWT) System (RENASYS EZ) for patients who would benefit from a suction device particulary as the device may promote wound healing.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1604-2014·2014-10-01

    Hospira Recalls Buprenorphine Hydrochloride Injection Due to Impurity Failure

    Hospira Inc. is recalling specific lots of Buprenorphine Hydrochloride Injection because the product failed impurity specifications during stability testing.

    Product
    BUPRENORPHINE HYDROCHLORIDE — BUPRENORPHINE HYDROCHLORIDE (BUPRENORPHINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighNHTSA·14V607000·2014-09-30

    Eldorado MST and Transmark Buses Recalled for Wheelchair Lift Defect

    Eldorado is recalling 2006-2007 MST and Transmark buses because wheelchair lift platform side plates may crack, posing an injury risk to operators.

    Product
    ELDORADO — ELDORADO MST, TRANSMARK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V611000·2014-09-30

    Diamond Coach Recalls 2006-2011 Buses with Cracking Wheelchair Lifts

    Diamond Coach is recalling 45 model year 2006-2011 PT and VIP buses because wheelchair lift platform side plates may crack, posing an injury risk.

    Product
    DIAMOND COACH — DIAMOND COACH PT, VIP
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V610000·2014-09-30

    Eldorado Recalls Coaches with Ricon Wheelchair Lifts Due to Cracking Risk

    Eldorado is recalling 2006-2014 coaches equipped with certain Ricon wheelchair lifts because the platform side plate may crack, posing an injury risk.

    Product
    ELDORADO — ELDORADO ADVANTAGE, AERO ELITE, AEROLITE, AEROTECH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14284·2014-09-30

    Trimfoot Recalls Children's Soft-Soled Sneakers Due to Choking Hazard

    Trimfoot is recalling First Impressions high-top soft-soled sneakers for infants because metal eyelets can detach and pose a choking hazard. No injuries have been reported.

    Product
    Children's soft-soled shoes
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14754·2014-09-30

    Husqvarna Recalls Craftsman Push Mowers Due to Injury Hazard

    Husqvarna is recalling about 700 Craftsman push mowers sold at Orchard Supply Hardware because the engine control lever can fail, posing an injury risk.

    Product
    Push lawn mowers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V608000·2014-09-30

    Campagna T-Rex 14 Motorcycle Recall for Engine Oil Pan Defect

    Campagna is recalling certain T-Rex 14 motorcycles because the engine oil pan may hit the road, causing an oil leak and loss of traction.

    Product
    T-REX — T-REX 14
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V606000·2014-09-29

    Navistar Recalls 2015 International TranStar Trucks for Clutch Nut Issue

    Navistar is recalling 78 model year 2015 International TranStar vehicles because a clutch rod nut may be missing or loose, which could cause the vehicle to lunge unexpectedly and increase crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL TRANSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide