The Recall Desk

State

US Virgin Islands product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

38626–38650 of 73916

  • ModerateFDA (Devices)·Z-1773-2018·2018-05-16

    Bard POWERPORT ClearVUE Slim Implantable Port Recalled for Incorrect Instructions

    Bard Peripheral Vascular Inc is recalling 10 units of POWERPORT ClearVUE Slim Implantable Port kits because the included Patient ID Card contains incorrect port flushing instructions.

    Product
    POWERPORT ClearVUE Slim Implantable Port with Smooth Septum and Attachable 8F Polyurethane Open-Ended Single-Lumen Venous Catheter Custom Kit, REF CP00005
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1677-2018·2018-05-16

    Siemens IMMULITE Assay Recalled Due to Biotin Interference Risk

    Siemens Healthcare Diagnostics is recalling specific IMMULITE assays because biotin can interfere with results, potentially affecting patient care.

    Product
    IMMULITE ¿ /IMMULITE ¿ 1000 BR-MA (CA15-3)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1680-2018·2018-05-16

    Siemens IMMULITE Gastrin Assay Recalled for Biotin Interference

    Siemens Healthcare Diagnostics is recalling IMMULITE Gastrin assays because biotin interference is not listed in the instructions for use.

    Product
    IMMULITE ¿ /IMMULITE 1000 ¿ Gastrin
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1691-2018·2018-05-16

    Siemens IMMULITE 2000 BR-MA (CA15-3) Assay Recalled for Biotin Interference

    Siemens Healthcare Diagnostics is recalling IMMULITE 2000 BR-MA (CA15-3) assays because biotin interference is not listed in the instructions for use.

    Product
    IMMULITE ¿ 2000/IMMULITE ¿ 2000 XPi BR-MA (CA15-3)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1631-2018·2018-05-16

    Randox Lipase Assay Recalled for Potential Contamination on Rx Instruments

    Randox Laboratories is recalling Lipase Assay kits due to potential contamination risks on Rx instruments. The recall affects specific lots distributed in West Virginia and Puerto Rico.

    Product
    Lipase, Catalog number: LI3837; GTIN: 05055273204230 and Catalog number: LI8361; GTIN: 05055273214284 Product Usage: For Professional Use for the quantitative in vitro determination of Lipase in human serum and plasma. Lipase measurements are used in the diagnosis and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0862-2018·2018-05-16

    Noven Recalls Minivelle Estradiol Patches Due to Adhesive Defect

    Noven Pharmaceuticals is recalling Minivelle (estradiol) transdermal systems because the adhesive may not meet specifications, causing patches to stick poorly to the skin.

    Product
    MINIVELLE — MINIVELLE (ESTRADIOL)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1760-2018·2018-05-16

    Bard POWERPORT ClearVUE Implantable Port Recalled for Incorrect Instructions

    Bard Peripheral Vascular Inc is recalling 359 units of POWERPORT ClearVUE implantable ports because the included patient ID card contains incorrect flushing instructions.

    Product
    POWERPORT(R) ClearVUE(R) isp with Smooth Septum, 6F ChronoFlex(TM), Polyurethane Catheter, REF 1666362
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1757-2018·2018-05-16

    Tornier Aequalis Humeral Nail Drill Bit Recall for Packaging Defect

    Tornier is recalling Aequalis Humeral Nail Drill Bits because the tips may puncture sterile packaging, potentially compromising sterility.

    Product
    AEQUALIS HUMERAL NAIL DRILL BIT, REF 7020140 Product Usage: The Aequalis Humeral Nail system is intended to provide temporary stabilization of various types of proximal and/or diaphyseal fractures of the humerus. Types of fractures include, but are not limited to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1780-2018·2018-05-16

    MHC Medical Recalls EasyTouch Insulin Syringes Due to Labeling Error

    MHC Medical Products LLC is recalling 46,600 EasyTouch insulin syringes because retail shelf cartons may display an incorrect lot number.

    Product
    EasyTouch (ET) Insulin Syringe 29G 0.5ml ¿" (Item 829555) Product Usage: INTENDED FOR INJECTION OF U100 INSULIN ONLY
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·18156·2018-05-15

    Regency Gas Stove Fireplaces Recalled for Explosion and Injury Hazards

    Regency is recalling U37 and U39 gas stove fireplaces because the pressure release system can fail, causing explosions and injuries.

    Product
    Regency Ultimate direct vent gas stove fireplaces (models U37 and U39)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·18V316000·2018-05-15

    Navistar Recalls 2018 IC Bus CE for Emergency Window Defect

    Navistar is recalling 2018 IC Bus CE transit buses because the emergency window release mechanism may be difficult to open, potentially hindering exit during an emergency.

    Product
    IC BUS — IC BUS CE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·18157·2018-05-15

    NY Thermal Recalls Residential and Commercial Boilers Due to Carbon Monoxide Hazard

    NY Thermal is recalling approximately 16,000 Trinity Tft and Slant/Fin CHS gas boilers because a deteriorating seal may allow carbon monoxide to leak into homes.

    Product
    NY Thermal (NTI) Trinity Tft and Slant/Fin CHS residential and commercial boilers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·18158·2018-05-15

    Michaels Recalls 3-Tier Haunted Townhouse Candle Holders Due to Fire Risk

    Michaels is recalling 3-Tier Haunted Townhouse candle holders because they can ignite, posing fire and burn hazards. One ignition incident was reported, with no injuries.

    Product
    3-Tier Haunted Townhouse candle holders
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereCPSC·18155·2018-05-14

    Harbor Freight Recalls 14-Inch Electric Chainsaws Due to Serious Injury Hazard

    Harbor Freight Tools is recalling approximately 1,020,000 14-inch electric chainsaws because the power switch can malfunction, allowing the saw to continue operating after being turned off.

    Product
    Portland, One Stop Gardens, and Chicago Electric 14 inch electric chainsaws
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V313000·2018-05-14

    Keystone Montana Fifth-Wheel Trailers Recalled for Fire Risk

    Keystone is recalling 2018 Montana fifth-wheel trailers because the slide-out room switch may lack circuit protection, increasing fire risk.

    Product
    KEYSTONE — KEYSTONE MONTANA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V312000·2018-05-14

    Ford Recalls 2018 Ecosport for Incorrect Brake Fluid Cap Labeling

    Ford is recalling 2018 Ecosport vehicles because they have European brake cap labels and manuals, which may confuse owners and affect brake performance.

    Product
    FORD — FORD ECOSPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V314000·2018-05-14

    BMW Recalls 2010-2011 335d Vehicles for Battery Cable Defect

    BMW is recalling 2010-2011 335d vehicles because a battery cable connection may degrade, causing intermittent power loss and unexpected stalling.

    Product
    BMW — BMW 335D
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V310000·2018-05-14

    Trail Boss Recalls One Horse Trailer Due to Propane Leak Risk

    Trail Boss is recalling one 2017 Twister Horse Trailer because a loose or missing propane gas valve screw may allow gas to leak, increasing fire risk.

    Product
    TRAIL BOSS — TRAIL BOSS TWISTER HORSE TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V309000·2018-05-13

    MCI Motor Coaches Recalled for Exhaust Pipe Fire Risk

    Motor Coach Industries is recalling 1,123 motor coaches because exhaust bellow pipes may develop holes, allowing hot gases to leak and increase fire risk.

    Product
    MCI — MCI D4000, D4500, D4005, D4505
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V308000·2018-05-11

    Kenworth Recalls 2018 T270 Trucks Due to Front Wheel Hub Defect

    PACCAR is recalling 2018 Kenworth T270 trucks because an incorrectly installed front wheel hub component may cause bearing failure and wheel separation.

    Product
    KENWORTH — KENWORTH T270
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V306000·2018-05-11

    Navistar Recalls 2019 International LT Trucks for Brake Drum Defect

    Navistar is recalling 2019 International LT heavy diesel trucks because lightweight brake drums may overheat, crack, or separate, increasing crash risk.

    Product
    INTERNATIONAL — INTERNATIONAL LT
    Category
    Vehicle
    Distribution
    Distributed nationwide