The Recall Desk

State

US Virgin Islands product recalls

73,817 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 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

48401–48425 of 73995

  • ModerateFDA (Devices)·Z-1874-2016·2016-06-08

    Philips Ingenuity Core 128 CT Systems Recalled for Drive Mapping Issue

    Philips Medical Systems is recalling 424 Ingenuity Core 128 CT systems because the system may not map the Varian drive after a user logout and login.

    Product
    Ingenuity Core 128 Computed Tomography X-ray Systems Product Usage: 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-1875-2016·2016-06-08

    Philips Ingenuity CT Systems Recalled for Drive Mapping Issue

    Philips is recalling 215 Ingenuity CT systems because they may fail to map the Varian drive after a user logs out and back in.

    Product
    Ingenuity Computed Tomography X-ray Systems Product Usage: 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-1839-2016·2016-06-08

    Baxter Recalls COSEAL Surgical Sealant Kits Due to Dissolution Issues

    Baxter Healthcare is recalling 6,804 units of COSEAL Surgical Sealant Kits because the PEG component may not fully dissolve, affecting hydrogel consistency.

    Product
    COSEAL Surgical Sealant Kit, 4 mL, Product Code: 934071; For use in vascular reconstructions to achieve adjunctive hemostasis by mechanically sealing areas of leakage.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0954-2016·2016-06-08

    Lupin Recalls Ceftriaxone Injection Vials Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling 570 vials of Ceftriaxone for Injection USP, 2 g, because the active pharmaceutical ingredients used in manufacturing failed specifications.

    Product
    Ceftriaxone for Injection USP, 2 g, Single Use Vial (NDC 68180-644-01) packaged in 10-count Vials per box (NDC 68180-644-10), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Mandideep…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0953-2016·2016-06-08

    Lupin Recalls Ceftriaxone Injection Vials Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection vials because they were manufactured using active pharmaceutical ingredients that failed specifications.

    Product
    Ceftriaxone for Injection USP, 1 g, Single Use Vial (NDC 68180-633-01) packaged in 10-count Vials per box (NDC 68180-633-10), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202; Manufactured by: Lupin Limited, Mandideep…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0952-2016·2016-06-08

    Lupin Recalls Ceftriaxone Injection Vials Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling Ceftriaxone for Injection USP, 500 mg, because the active ingredients used in manufacturing failed specifications.

    Product
    Ceftriaxone for Injection USP, 500 mg, Single Use Vial, packaged in a) 1-count Vials per box (NDC 68180-622-01), and b) 10-count Vials per box (NDC 68180-622-10), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0951-2016·2016-06-08

    Lupin Recalls Ceftriaxone Injection Vials Due to CGMP Deviations

    Lupin Pharmaceuticals is recalling specific lots of Ceftriaxone for Injection USP because they were manufactured using active pharmaceutical ingredients that failed specifications.

    Product
    Ceftriaxone for Injection USP, 250 mg, Single Use Vial, packaged in a) 1-count Vials per box (NDC 68180-611-01), and b) 10-count Vials per box (NDC 68180-611-10), Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., 111 South Calvert Street, Baltimore, Maryland 21202…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1907-2016·2016-06-08

    B. Braun Recalls Non-Vented Dispensing Pins Due to Packaging Tears

    B. Braun Medical is recalling 11,000 Non-Vented Dispensing Pins because the outer blister packaging may tear, potentially compromising the device.

    Product
    Non-Vented Dispensing Pin with Luer Lock Ultrasite Valve Product Usage: Used for aspiration of medication from inverted bags or semi-rigid containers. Interavenous delivery of transferred medication(Device is not intended for direct infusion)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0955-2016·2016-06-08

    Lupin Recalls Ceftriaxone Sodium API Due to CGMP Deviations

    Lupin Pharmaceuticals Inc. is recalling Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient because intermediates failed specifications.

    Product
    Ceftriaxone Sodium (Sterile) USP active pharmaceutical ingredient, DMF No. 15931; Manufactured by: Lupin Limited, Unit-1, 198-202, New Industrial Area No. 2, Dist. Raisen, Mandideep-462 046, (Madhya Pradesh) India; Regd. Office: 159, CST Road Kalina, Santacruz (E), Mumbai- 400…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1906-2016·2016-06-08

    B. Braun Medical Recalls Non-Vented Dispensing Pins Due to Packaging Tears

    B. Braun Medical is recalling approximately 11,000 Non-Vented Dispensing Pins because the outer blister packaging may tear, potentially compromising the product label.

    Product
    Non-Vented Dispensing Pin with One-Way Valve and Luer Lock Ultrasite Valve Product Usage: Used for aspiration of medication from inverted bags or semi-rigid containers. Interavenous delivery of transferred medication(Device is not intended for direct infusion)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·16752·2016-06-07

    Focus Bicycles Recalls Spine Models Due to Frame Collapse Risk

    Focus Bicycles is recalling about 80 Spine mountain bicycles because incorrectly sized seatstay or linkage parts can cause the frame to collapse, posing a fall hazard.

    Product
    Focus Spine bicycles
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·16V407000·2016-06-07

    Thomas Built Buses Recall Emergency Door Handle Corrosion Defect

    Daimler Trucks North America is recalling 717 Thomas Built Buses because corrosion on the emergency door handle stem could delay evacuation during an emergency.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES, THOMAS CL-960, SAF-T-LINER MVP-ER, SAF-T-LINER CONVENTIONAL, TL-960
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V404000·2016-06-06

    Lakota Recalls 2016 Trailers Due to Aluminum Rim Pin Holes

    Lakota is recalling 2016 Bighorn, Charger, and Livestock Edition trailers because pin holes in aluminum rims may cause tire failure and increase crash risk.

    Product
    LAKOTA — LAKOTA BIGHORN, LIVESTOCK EDITION
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16E052000·2016-06-06

    Meritor Recalls Front Axles Due to Potential Heat Treatment Defect

    Meritor is recalling specific FF967 Non-Drive Front Steer axles manufactured in 2012 because they may have been incorrectly heat treated, posing a risk of fracture and loss of vehicle control.

    Product
    SUSPENSION:FRONT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V403000·2016-06-06

    Volkswagen Recalls 2016 Jetta, Passat, and Golf for Fuel Rail Defect

    Volkswagen is recalling specific 2016 Jetta, Passat, and Golf vehicles because the fuel rail may detach, causing a fuel leak that could lead to a vehicle fire.

    Product
    VOLKSWAGEN — VOLKSWAGEN GOLF, JETTA, PASSAT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V405000·2016-06-06

    Blue Bird Recalls Transit Buses with Defective Wheelchair Lifts

    Blue Bird is recalling 2015-2017 All American and 2016-2017 Vision transit buses equipped with Ricon S-Series wheelchair lifts due to potential platform cracking and bearing displacement.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V401000·2016-06-03

    Chrysler Sebring and Dodge Stratus Recall for Sun Visor Tether Defect

    Mitsubishi is recalling 2001-2002 Chrysler Sebring and Dodge Stratus vehicles with beige interiors because an incorrect part may allow the passenger sun visor to detach during airbag deployment.

    Product
    CHRYSLER — CHRYSLER, DODGE SEBRING, STRATUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V400000·2016-06-03

    Spartan Gladiator and MetroStar Emergency Vehicles Recalled for Pump Defect

    Spartan is recalling 2015 Gladiator and MetroStar emergency vehicles because improperly soldered pump strainers may break, potentially damaging the pump and reducing firefighting effectiveness.

    Product
    SPARTAN — SPARTAN GLADIATOR, METROSTAR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·16751·2016-06-02

    Hillsdale Furniture Recalls Children's Bunk Beds Due to Fall Hazard

    Hillsdale Furniture is recalling about 20,000 children's bunk beds sold at Bob's Discount Furniture because support rails can crack or break, posing a fall hazard.

    Product
    Children's bunk beds
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V399000·2016-06-02

    West-Mark Recalls 2014-2015 Sugar Tank Trailers Due to Brake Drag

    West-Mark is recalling 2014-2015 Sugar Tank trailers because improperly seated brake diaphragms may cause drag, potentially leading to wheel end fires.

    Product
    WEST-MARK — WEST-MARK SUGAR TANK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V397000·2016-06-02

    Tiffin Allegro Motorhomes Recalled for Steering Box Wear Risk

    Tiffin is recalling 2014-2016 Allegro motorhomes because incorrect steering box spacers can cause premature wear, leading to a sudden loss of steering ability and increased crash risk.

    Product
    TIFFIN — TIFFIN ALLEGRO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·16V394000·2016-06-02

    Autocar Recalls 2016-2017 Xpeditor Trucks for Engine Stall Risk

    Autocar is recalling 18 Xpeditor trucks due to a defective engine control module that may cause the engine to stall unexpectedly, increasing crash risk.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide