The Recall Desk

State

US Virgin Islands product recalls

73,741 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 73,741 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

40826–40850 of 73919

  • SevereFDA (Drugs)·D-0013-2018·2017-10-25

    Alprazolam Tablets Recalled for Unknown Impurity

    The Harvard Drug Group is recalling Alprazolam Tablets, 0.25 mg, due to an out-of-specification result for an unknown impurity.

    Product
    Alprazolam Tablets, USP, 0.25 mg, 100-count Unit Dose tablets per carton, Rx Only, Manufactured by: Watson Pharma Private Limited, Verna, Salcette Goa 403 722 INDIA; Distributed by: Actavis Pharma, Inc., Parsippany, NJ 07054; Distributed by: Major Pharmaceuticals, 17177 N.…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V676000·2017-10-25

    BMW Recalls 2006-2011 3 Series Vehicles for Fire Risk

    BMW is recalling 2006-2011 3 Series vehicles because heating and air conditioning wiring may overheat, increasing the risk of a fire.

    Product
    BMW — BMW 325XI, 323I, 325I, 328I
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0028-2018·2017-10-25

    Death Wish Nitro Canned Cold Brew Coffee Recalled for Botulism Risk

    Death Wish Coffee Company is recalling 80,777 cans of Nitro Canned Cold Brew Coffee nationwide due to a potential for Clostridium Botulinum.

    Product
    Death Wish Nitro Canned Cold Brew Coffee 11 oz UPC: 851552005599
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0023-2018·2017-10-25

    St. Jude Medical Recalls Infinity 5 and 7 Implantable Pulse Generators

    St. Jude Medical is recalling 3,119 Infinity 5 and 7 Implantable Pulse Generators because battery longevity estimations may be inaccurate.

    Product
    Infinity 5 Implantable Pulse Generator and Infinity 7 Implantable Pulse Generator Models 6660, 6661, 6662, 6663
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·17V675000·2017-10-25

    Audi Recalls A4 and A5 Models for Loose Door Speaker Trim

    Volkswagen Group of America is recalling 2017-2018 Audi A4 and A5 vehicles because loose aluminum door trim can expose sharp edges, increasing the risk of injury to occupants.

    Product
    AUDI — AUDI A5, A4 ALLROAD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0022-2018·2017-10-25

    St. Jude Medical Recalls Proclaim Elite Implantable Pulse Generators

    St. Jude Medical is recalling 28,817 Proclaim 5 and 7 Elite Implantable Pulse Generators because battery longevity estimations may be inaccurate.

    Product
    Proclaim 5 Elite Implantable Pulse Generator and Proclaim 7 Elite Implantable Pulse Generator Models 3660, 3661, 3662, 3663, 3665, 3667
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0026-2018·2017-10-25

    CareFusion Recalls Alaris Pump Modules Due to Flow Rate Variations

    CareFusion 303, Inc. is recalling Alaris Pump Module model 8100 units due to reports of increased or decreased medication flows.

    Product
    Alaris Pump Module model 8100 manufactured between November 2011 and March 2012; Alaris Pump Module serviced with LVP Mechanism Sub Assembly (P/N) 10942012 between November 2011 and March 2012; Alaris Pump module Bezel Kit Assembly (P/N) 10964559) shipped between November…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0029-2018·2017-10-25

    Bel Brands Recalls Merkts Port Wine Cheese Spread Due to Foreign Material

    Bel Brands USA is recalling Merkts Port Wine Cheese Spread after customers reported finding white plastic pieces in the product.

    Product
    Merkts Port Wine Cheese Spread, Net Wt. 14 oz (396g), UPC 76306-60200
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·18016·2017-10-25

    PlanToys Recalls Baby Gyms Due to Strangulation Hazard

    PlanToys is recalling about 500 baby gyms sold in 2016 and 2017 because babies can strangle on the side rope crossbars. No injuries have been reported.

    Product
    Baby Gym
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0025-2018·2017-10-25

    Medtronic Recalls VCLAS Laser Applicators Due to Saline Leakage Testing Defect

    Medtronic is recalling 423 VCLAS laser applicator systems because they were not appropriately tested for saline leakage during manufacturing.

    Product
    VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559 Visualase Cooled Laser Applicator System 3mm Tip; Part Number: 9735560 Visualase Cooled Laser Applicator System 10mm Tip; Part Number: 9735561 Visualase Cooled Laser Applicator System 15mm Tip
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0010-2018·2017-10-25

    Unichem Recalls Bisoprolol Fumarate Tablets Due to Stability Impurity

    Unichem Pharmaceuticals is recalling 96,876 bottles of Bisoprolol Fumarate 5 mg tablets because stability testing revealed an out-of-specification unknown impurity.

    Product
    BISOPROLOL FUMARATE — BISOPROLOL FUMARATE (BISOPROLOL FUMARATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0020-2018·2017-10-25

    Philips Brilliance iCT SP CT Systems Recalled for Image Reconstruction Failure

    Philips is recalling Brilliance iCT SP CT systems because a software defect prevents image reconstruction after bolus tracking scans, potentially requiring patients to be rescanned.

    Product
    Philips Healthcare Brilliance iCT SP X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0015-2018·2017-10-25

    Philips Brilliance 64 CT Systems Recalled for Image Reconstruction Failure

    Philips Electronics North America Corporation is recalling 606 Brilliance 64 CT systems in the US because a software defect prevents image reconstruction after certain scans.

    Product
    Philips Healthcare Brilliance 64 System, X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0016-2018·2017-10-25

    Philips Ingenuity Core CT Systems Recalled for Image Reconstruction Failure

    Philips is recalling 606 Ingenuity Core CT systems in the US because a software defect prevents image reconstruction after bolus tracking scans.

    Product
    Philips Healthcare Ingenuity Core X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0039-2018·2017-10-25

    Teleflex Pilling Knife Handles Recalled for Blade Fit Issues

    Teleflex Medical is recalling Pilling Knife Handles because the slot depth is out of specification, which may prevent blades from fitting properly.

    Product
    Pilling Knife Handles: a) REF 352950 b) REF 352953 c) REF 352951 d) REF 352957 e) REF 352952 : Reusable surgical knife handles, which are intended for use with blades which are inserted into a slot in the handle.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0019-2018·2017-10-25

    Philips Brilliance iCT CT Scanner Recall for Data Reconstruction Failure

    Philips is recalling Brilliance iCT CT scanners because a software defect prevents image reconstruction after bolus tracking scans, potentially requiring patients to be rescanned.

    Product
    Philips Healthcare Brilliance iCT X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0012-2018·2017-10-25

    Toshiba Medical Kalare Fluoroscopic X-Ray System Recalled for Image Display Failure

    Toshiba American Medical Systems Inc is recalling 96 Kalare Fluoroscopic X-Ray Systems because images may fail to display on the system monitor or save to the hard disk.

    Product
    Toshiba Medical Kalare Fluoroscopic X-Ray System (DREX-KL80) Kalare is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic examinations, including general R&F and pediatric examinations. It is intended for use by…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0018-2018·2017-10-25

    Philips Ingenuity Core128 CT Systems Recalled for Image Reconstruction Failure

    Philips is recalling Ingenuity Core128 CT systems because a software defect prevents image reconstruction after bolus tracking scans, potentially requiring patient rescans.

    Product
    Philips Healthcare Ingenuity Core128 X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0017-2018·2017-10-25

    Philips Ingenuity CT Systems Recalled for Bolus Tracking Image Failure

    Philips is recalling Ingenuity CT systems because a software defect prevents image generation during bolus tracking procedures, potentially requiring patient rescans.

    Product
    Philips Healthcare Ingenuity CT X-Ray, Tomography, Computed These computed tomography x-ray systems are intended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V670000·2017-10-24

    2018 Jeep Cherokee and Compass Recall for Oil Pump Housing Defect

    Chrysler is recalling 2018 Jeep Cherokee and Compass vehicles with 2.4L engines due to a cracked oil pump housing that can cause engine stalling and increase crash risk.

    Product
    JEEP — JEEP CHEROKEE, COMPASS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18015·2017-10-24

    Fisher-Price Recalls Soothing Motions Seats Due to Fire Hazard

    Fisher-Price is recalling Soothing Motions Seats because the motor housing can overheat, posing a fire hazard. No injuries have been reported.

    Product
    Soothing Motions Seats
    Category
    Consumer Product
    Distribution
    Distributed nationwide