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.

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.

57876–57900 of 74005

  • ModerateFDA (Devices)·Z-2017-2014·2014-07-16

    Teleflex Medical Recalls Humidifier Adaptors Due to Packaging Seal Issues

    Teleflex Medical is recalling 7.7 million Humidifier Adaptors because creased packaging seals may affect integrity. The products were distributed in the US and 12 other countries.

    Product
    Humidifier Adaptor, 040 Shelf Pak, French, Teleflex Medical, respiratory gas humidifier adaptor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1426-2014·2014-07-16

    Ferring Recalls Endometrin Vaginal Inserts Due to Discoloration

    Ferring Pharmaceuticals is recalling 72,046 cartons of Endometrin vaginal inserts nationwide due to discoloration caused by heat exposure.

    Product
    ENDOMETRIN — ENDOMETRIN (PROGESTERONE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2009-2014·2014-07-16

    Teleflex Medical Recalls Aquapak 340 SW Respiratory Gas Humidifier Adaptors

    Teleflex Medical is recalling Aquapak 340 SW respiratory gas humidifier adaptors because creased packaging seals may affect integrity.

    Product
    Aquapak 340 SW, 340, mL w/040 Adaptor, Japan, Teleflex Medical, respiratory gas humidifier adaptor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2007-2014·2014-07-16

    Teleflex Medical Recalls Aquapak SW/EAU Respiratory Gas Humidifier Adaptors

    Teleflex Medical is recalling Aquapak SW/EAU respiratory gas humidifier adaptors because creased packaging seals may affect integrity.

    Product
    Aquapak SW/EAU, Sterile, 340 mL, w/Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2013-2014·2014-07-16

    Teleflex Medical Recalls Aquapak 640 SW Respiratory Gas Humidifier Adaptors

    Teleflex Medical is recalling Aquapak 640 SW respiratory gas humidifier adaptors because creased packaging seals may affect integrity. The recall covers units distributed in the US and 11 other countries.

    Product
    Aquapak 640 SW, 650 mL w/040 Adaptor, French, Teleflex Medical, respiratory gas humidifier adaptor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2036-2014·2014-07-16

    Steris Recalls Reliance 1227 Washer Due to Door Handle Pin Deformation

    Steris is recalling 37 Reliance 1227 Cart and Utensil Washer/Disinfector units because the door handle pin may deform or break, potentially rendering the door inoperable.

    Product
    Reliance 1227 Cart and Utensil Washer/Disinfector Product Usage: Usage: The Reliance 1227 Cart and Utensil Washer/Disinfector is intended for use in the cleaning and low-level disinfection of bedpans and urinals, basins, carts, beds, theater shoes and other miscellaneous…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2018-2014·2014-07-16

    Terumo Advanced Perfusion System 1 Recall for Manual Clarity Issues

    Terumo is recalling 1,713 Advanced Perfusion System 1 units because the operator manual lacks clarity and accuracy.

    Product
    Terumo¿ Advanced Perfusion System 1 100/120V AC, Advanced Perfusion System Platform (APS)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2015-2014·2014-07-16

    Teleflex Medical Recalls Respiratory Gas Humidifier Adaptors Due to Packaging Seal Issues

    Teleflex Medical is recalling 7,758,650 respiratory gas humidifier adaptors because creased packaging seals may affect integrity. The recall covers units distributed in the US and 11 other countries.

    Product
    Adaptor, 040 Hum, International, Teleflex Medical, respiratory gas humidifier adaptor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2004-2014·2014-07-16

    Teleflex Medical Recalls Aquapak Respiratory Gas Humidifier Adaptors for Packaging Defects

    Teleflex Medical is recalling Aquapak 640 SW and 650 mL respiratory gas humidifier adaptors because creased packaging seals may affect integrity.

    Product
    Aquapak 640 SW, 650, mL w/040 Adaptor, International, Teleflex Medical, respiratory gas humidifier adaptor .
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2006-2014·2014-07-16

    Teleflex Medical Recalls Aquapak 340 SW Respiratory Gas Humidifier Adaptors

    Teleflex Medical is recalling Aquapak 340 SW respiratory gas humidifier adaptors because creased packaging seals may affect integrity. The recall covers units distributed in the US and 12 other countries.

    Product
    Aquapak 340 SW, 340, mL w/040 Adaptor, Teleflex Medical, respiratory gas humidifier adaptor.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V425000·2014-07-14

    Aston Martin Recalls 2014 DB9 and Rapide S for Transmission Defect

    Aston Martin is recalling 440 model year 2014 DB9 and Rapide S vehicles because a faulty circuit board may cause the transmission to shift to neutral without driver input.

    Product
    ASTON MARTIN — ASTON MARTIN DB9, RAPIDE S
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E040000·2014-07-14

    PACCAR Recalls Mirrex and TRP Warning Triangle Kits for Missing Markings

    PACCAR is recalling aftermarket Mirrex and TRP warning triangle kits sold between 2009 and 2014 because they lack required manufacturer markings, failing to meet federal safety standards.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V422000·2014-07-14

    BMW Recalls 2014 i3 and MINI Cooper for Air Bag Defect

    BMW is recalling certain 2014 i3 and MINI Cooper vehicles because the front passenger air bag inflator may not be assembled correctly, potentially preventing proper deployment in a crash.

    Product
    BMW — BMW, MINI I3, COOPER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E038000·2014-07-11

    Tucker Rocky Recalls Cyber River Road Grateful Dead U-6 Motorcycle Helmets

    Tucker Rocky is recalling specific Cyber River Road Grateful Dead U-6 motorcycle helmets because they failed federal safety impact tests. Owners should contact the company for a free replacement.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E037000·2014-07-10

    Airtex E84070 Replacement Fuel Pumps Recalled for Leak Risk

    UCI-Fram Group is recalling Airtex E84070 replacement fuel pumps shipped between December 2013 and June 2014 due to a seal defect that may cause fluid leaks and increase fire risk.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14228·2014-07-10

    Gemini Recalls Power Adaptor Chargers Due to Burn Hazard

    Gemini is recalling about 31,000 promotional power adaptors/chargers because they can overheat and cause burns. Consumers should stop using and dispose of the units.

    Product
    Power adaptor/chargers (promotional giveaway)
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V419000·2014-07-10

    Nissan Recalls 2014 NV Vans Due to Seat Belt Bolt Defect

    Nissan is recalling 2014 NV vans because seat belt retractor bolts may be loose or missing, potentially compromising occupant restraint in a crash.

    Product
    NISSAN — NISSAN NV
    Category
    Vehicle
    Distribution
    Distributed nationwide