The Recall Desk

State

US Virgin Islands product recalls

73,570 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.

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26876–26900 of 73748

  • SevereNHTSA·20V722000·2020-11-20

    Triple E Recalls Motorhomes Due to Chafed Wire Harness and Tail Light Loss

    Triple E is recalling 2018-2021 Unity and Serenity motorhomes because a shifting water tank bracket can chafe the wire harness, causing tail lights to fail and increasing crash risk.

    Product
    TRIPLE E — TRIPLE E UNITY, SERENITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V725000·2020-11-20

    2021 Honda Pilot Tire Safety Recall Due to Over-Curing Defect

    Honda is recalling 2021 Pilot vehicles with certain Continental tires that may be over-cured, potentially causing sidewall breaks or belt separation leading to loss of vehicle control. Dealers will replace affected tires free of charge.

    Product
    HONDA — HONDA PILOT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V726000·2020-11-20

    2021 Lincoln Aviator steering knuckle defect increases crash risk

    Ford is recalling certain 2021 Lincoln Aviator vehicles due to improperly manufactured steering knuckles that may fracture, reducing steering control and increasing crash risk. Dealers will inspect and replace affected knuckles free of charge.

    Product
    LINCOLN — LINCOLN AVIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V719000·2020-11-20

    Newmar Motorhomes Recalled for Cooking Stove Gas Leak Fire Risk

    Newmar motorhomes equipped with Dometic 3-burner cooking stoves may have an overtightened saddle valve bolt that damages the seal, causing a gas leak and increasing fire risk. Owners should contact Newmar for a free remedy.

    Product
    NEWMAR — NEWMAR VENTANA, VENTANA LE, BAY STAR, DUTCH STAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V718000·2020-11-19

    2021 Thor Motor Coach Four Winds motorhomes recalled for stove gas leak

    Thor Motor Coach is recalling certain 2021 Four Winds motorhomes with Dometic stoves due to a potential gas leak that could increase fire risk. The stove's saddle valve bolt may be overtightened, damaging the seal.

    Product
    THOR MOTOR COACH — THOR MOTOR COACH FOUR WINDS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21709·2020-11-19

    Polaris Recalls RZR Recreational Off-Highway Vehicles Due to Clutch Failure Hazard

    Polaris is recalling about 18,400 RZR recreational off-highway vehicles because the clutch can fail, posing an injury hazard. No injuries have been reported.

    Product
    Model Years 2020-2021 RZR PRO XP, PRO XP4 and Model Year 2021 RZR Turbo S, Turbo S4, XP Turbo and XP 4 Turbo ROV
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0115-2021·2020-11-18

    Starwest Botanicals Recalls Organic Elderberry Due to Salmonella Risk

    Starwest Botanicals is recalling organic elderberry because a customer test detected Salmonella. The product was distributed nationwide and to two Canadian customers.

    Product
    Elderberry Whole Organic; Sambucus Nigra; Origin: Croatia Distributed in boxes with plastic liners. Various sizes Bulk UPC 7 67963 07314 3, Item # 209290-00 Starwest Botanicals,Inc. 161 Main Street, Sacramento, CA 95838 Certified Organic
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0425-2021·2020-11-18

    Puritan Bennett 980 Ventilator Recalled for Battery Overheating Risk

    Covidien is recalling Puritan Bennett 980 ventilators due to battery overheating and thermal damage risks that could cause burns or smoke exposure.

    Product
    Puritan Bennett 980 (PB980) Ventilator Series - Product Usage: for use on patient population sizes from Neonatal (NICU) through Adult who require respiratory support or mechanical ventilation SKU: 980X1ENDIUU 980X1ENDIUU 980X3FRAIQC 980X3DEDRAC 980X3ENNISB 980X3NLDRAC…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V714000·2020-11-18

    Alfa Romeo Giulia Recall for Rear Brake Disc Fracture Risk

    FCA US LLC is recalling 2020 Alfa Romeo Giulia vehicles because rear brake discs may fracture, potentially reducing braking performance and increasing crash risk.

    Product
    ALFA ROMEO — ALFA ROMEO GIULIA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0072-2021·2020-11-18

    H & H Remedies Recalls White Liniment Due to CGMP Deviations

    H & H Remedies, LLC is voluntarily recalling 365 bottles of White Liniment due to Current Good Manufacturing Practice (CGMP) deviations.

    Product
    White Liniment packaged in a) 1 oz; b) 4 oz.; and c) 6 oz bottles. Mfg & Sold by: H & H Remedies, LLC c/o David A. Cox, 1219 South Broadway, New Philadelphia, OH 44663
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V715000·2020-11-18

    Keystone Outback trailers recalled for potential frame rail buckling defect

    Keystone is recalling 2019–2021 Outback recreational trailers for inadequate frame rail support that may cause buckling and crash risk. Owners should contact 1-866-425-4369 for the free frame reinforcement repair.

    Product
    KEYSTONE — KEYSTONE OUTBACK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V713000·2020-11-18

    Lamborghini Recalls 2019-2020 Urus Vehicles Due to Fuel Line Fire Risk

    Lamborghini is recalling 2,831 2019-2020 Urus vehicles because high engine temperatures may damage the fuel line connector, causing a leak and increasing fire risk.

    Product
    LAMBORGHINI — LAMBORGHINI URUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0431-2021·2020-11-18

    Stryker Recalls Cranial Perforators Due to Potential Metal Fragment Risk

    Stryker is recalling Zyphr Disposable Cranial Perforators because a crack in the inner bit could release metal fragments into the surgical site or cause delayed disengagement.

    Product
    Stryker Zyphr Disposable Cranial Perforator, Large 14/11 mm- is a sterile, single use cutting accessory intended for cutting an 11 mm diameter access hole through the cranium of adult patients. Catalog Number: 5100-060-001
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0076-2021·2020-11-18

    Baxter Recalls Bupivacaine Injection Due to Particulate Matter

    Baxter Healthcare is recalling specific lots of Bupivacaine Hydrochloride Injection due to the presence of black and transparent particles in the solution.

    Product
    Bupivacaine Hydrochloride in 8.25% Dextrose Injection, USP Spinal 0.75% (15 mg/2 mL) 10 x 2 mL single-dose ampules, Rx only, Manufactured for: Baxter Healthcare Corporation Deerfield, IL 60015 USA, Manufactured by: Baxter Pharmaceuticals India Private Ltd Ahmedabad 382213 India…
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0439-2021·2020-11-18

    Fresenius Liberty Select Cycler Software Recall for Inadequate Dialysis Risk

    Fresenius Medical Care is recalling Liberty Select Cycler devices with software version 2.9.0 because a software error may cause the device to fail to recognize extra fluid, potentially leading to inadequate dialysis.

    Product
    Liberty Select Cycler Software Version 2.9.0 Model Number 180343 and RTLR180343
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0446-2021·2020-11-18

    United Imaging uCT 550 CT Scanners Recalled for Timer Display Error

    Shanghai United Imaging Healthcare is recalling five uCT 550 CT scanners because an incorrect delay timer display may expose operators to unnecessary radiation.

    Product
    Computed Tomography X-Ray System, Model uCT 550, Rx, CE, GTIN: 06971576831036 - Product Usage: ntended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0445-2021·2020-11-18

    United Imaging uCT 530 CT Scanner Recalled for Incorrect Timer Display

    Shanghai United Imaging Healthcare Co., Ltd. is recalling four uCT 530 CT scanners because an incorrect delay timer may display, potentially exposing operators to unnecessary radiation.

    Product
    Computed Tomography X-Ray System, Model uCT 530, Rx, CE, GTIN: 06971576831012 - Product Usage: ntended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0427-2021·2020-11-18

    Boston Scientific AMS 700 MS Pump Recall for Activation Difficulties

    Boston Scientific is recalling AMS 700 MS Pumps due to reports of difficulty activating the device to inflate cylinders.

    Product
    AMS 700 MS Pump with and without InhibiZone, sold as individual units and also pre-connected to AMS 700 cylinders. Inflatable Penile Prosthesis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0447-2021·2020-11-18

    United Imaging uCT 760 CT Scanner Recalled for Timer Display Error

    Shanghai United Imaging Healthcare is recalling five uCT 760 CT scanners because a display error may cause operators to receive unnecessary radiation exposure.

    Product
    Computed Tomography X-Ray System, Model uCT 760, Rx, CE, GTIN: 06971576831043 - Product Usage: ntended to produce cross-sectional images of the body by computer reconstruction of x-ray transmission data taken at different angles and planes and indicated for the whole body…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0448-2021·2020-11-18

    United Imaging uMI 550 PET/CT System Recalled for Incorrect CT Scan Delay Timer

    Shanghai United Imaging Healthcare is recalling nine uMI 550 PET/CT systems because an incorrect CT scan delay timer may display, potentially exposing operators to unnecessary radiation.

    Product
    Positron Emission Tomography and Computed Tomography System, Model uMI 550, Rx, CE, GTIN: 06971576832026 - Product Usage: intended to be operated by qualified healthcare professionals to assist in the detection, localization, diagnosis, staging, restaging, treatment planning…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0443-2021·2020-11-18

    Maquet BMU 40 Blood Monitoring Units Recalled for Electrical Safety Non-Compliance

    Maquet Cardiovascular is recalling 51 Blood Monitoring Units (BMU 40) because the printed circuit boards do not meet IEC electrical safety standards for creepage distance.

    Product
    Blood Monitoring Unit (BMU 40), model no. 701040852 - Product Usage: is to monitor blood parameters during cardiopulmonary bypass (CPB) or similar procedures with extracorporeal circulation, which require continuous monitoring of the arterial and/or venous blood parameters…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·20V716000·2020-11-18

    2021 Volkswagen Atlas and Select Models: Rear Camera Malfunction Risk

    Volkswagen is recalling certain 2021 Atlas and related models because the rear view camera may malfunction during startup, showing a black screen or frozen image, reducing visibility when reversing and increasing crash risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN ARTEON, GOLF, JETTA, TIGUAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0114-2021·2020-11-18

    Starwest Botanicals Recalls Organic Elderberry Tea Due to Salmonella Risk

    Starwest Botanicals is recalling specific lots of organic elderberry tea after a customer test detected Salmonella.

    Product
    Elderberry Whole Organic; Sambucus Nigra; Origin: Croatia 1 lb. and 4 oz. Distributed in Mylar bags. 1 lb. UPC: 7 67963 07315 0; Item # 209290-01 4 oz. UPC 7 67963-10561-5; Item # 209290-04 Daily serving size; Pour 8-12 oz. of boiling water (212 degrees F) over 1 tsp…
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0069-2021·2020-11-18

    Teva Recalls Mesalamine Tablets Due to Failed Dissolution Testing

    Teva Pharmaceuticals is recalling 133,829 bottles of Mesalamine Delayed-Release Tablets because stability testing revealed out-of-specification dissolution results.

    Product
    MESALAMINE — MESALAMINE (MESALAMINE)
    Category
    Drug
    Distribution
    Distributed nationwide