The Recall Desk

State

US Virgin Islands product recalls

73,833 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 73,833 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

59401–59425 of 74011

  • ModerateFDA (Devices)·Z-1019-2014·2014-02-26

    Zimmer Recalls Bipolar Liners and Multipolar Cups Due to Packaging Validation Issues

    Zimmer is recalling 7,044,680 units of bipolar liners and multipolar cups because packaging operations at a Puerto Rico facility were not properly validated, despite passing subsequent seal integrity tests.

    Product
    Bipolar liners and Multipolar cups with the following dimensions in MM (38, 39, 40, 41, 42, 43, 44, 45, 46, 47, 48, 49, 50, 53, 54, 55, 57, 58, 60, 64, 66, 68, 70, 72) and several OD
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1035-2014·2014-02-26

    Zimmer Recalls Modular Hip Implants Due to Packaging Validation Issues

    Zimmer is recalling specific lots of Modular Austin Moore and Moore Hip ProS hip implants because packaging operations at a Puerto Rico facility were not properly validated.

    Product
    MODULAR AUSTIN MOORE SOLI and MOORE HIP PROS REG SOLID
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0986-2014·2014-02-26

    Synthes 3.2 mm Guide Wire Recalled for Incorrect Raw Material Labeling

    Synthes, Inc. is recalling 3.2 mm Guide Wires because the label lists an incorrect raw material. The recall covers units distributed in the USA, Canada, and Switzerland.

    Product
    Synthes 3.2 mm Guide Wire 400mm. Used for guiding the TFN Helical Blade and TFN Lag Screw into the femoral.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1022-2014·2014-02-26

    Zimmer Recalls NEXGEN Knee Implant Components Due to Packaging Validation Issues

    Zimmer is recalling NEXGEN knee implant components because packaging operations at its Puerto Rico facility were not properly validated, despite passing subsequent seal integrity tests.

    Product
    NEXGEN MIS TIBIA PLATE PR NEXGEN TAPER PLUG NEXGEN PRECOAT PEG TIB PL NEXGEN MICRO ALL-POLY PAT NEXGEN ALL-POLY PATELLA, NEXGEN PRECOAT STEMMED TI NEXGEN OPTION STEMMED TIB NEXGEN STRAIGHT STEM EXT NEXGEN SHARP FLUTED STEM NEXGEN FLUTED STEM EXT, 1 NEXGEN…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1004-2014·2014-02-26

    Zimmer Recalls Sterile Orthopedic Screws Due to Packaging Validation Issues

    Zimmer is recalling specific sterile orthopedic screws because packaging operations at a Puerto Rico facility were not properly validated, despite passing seal integrity tests.

    Product
    Item codes starting with 001930 LAG SCR 12.7D X 55MM SHOR up to 155 MM, LAG SCR 12.7D X 55 MM SHO up to 100MM, LAG SCR 12.7D X 55MM STAN up to 155 MM, LAG SCR 15.8D X 55MM LARG up to 155 MM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1001-2014·2014-02-26

    Zimmer Recalls Magna-Fx Cannulated Screws Due to Packaging Validation Issues

    Zimmer is recalling Magna-Fx Cannulated Screw Fixation Systems because packaging operations at a Puerto Rico facility were not properly validated, despite passing subsequent seal integrity tests.

    Product
    Magna-Fx Cannulated Screw Fixation System 7.0 mm. Item codes starting with 0011420, 11460 and 11461.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1025-2014·2014-02-26

    Zimmer Recalls HGP II Acetabular Cup Due to Packaging Validation Issues

    Zimmer is recalling HGP II Acetabular Cup Bon due to unvalidated packaging operations at its Puerto Rico facility, despite passing seal integrity tests.

    Product
    HGP II ACETABULAR CUP BON
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1017-2014·2014-02-26

    Zimmer Recalls Hip Prostheses Due to Packaging Validation Issues

    Zimmer, Inc. is recalling specific hip prosthesis models because packaging operations at a Puerto Rico facility were not properly validated, raising concerns about sterile barrier integrity.

    Product
    MOORE HIP PROS LONG FENES, MOORE HIP PROS NRW STR FE, MOORE HIP PROS STR FENEST, THOMPSON HIP PROSTHESIS sizes 3, 4, 5, and 6, and Mod Austin Moore Fem Stem
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1063-2014·2014-02-26

    Implantech Recalls Gelzone Shoulder Sleeves Due to Velcro Closure Defect

    Implantech Associates Inc is voluntarily recalling Gelzone Shoulder Sleeves because the Velcro closure may not meet robustness requirements.

    Product
    Gelzone Shoulder Sleeve, Catalog Number SLV634, Lot Number 852766. Product Usage: To be used where limb support and/or elevation is considered necessary.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1038-2014·2014-02-26

    Zimmer Recalls Bone Screws Due to Unvalidated Packaging Operations

    Zimmer is recalling 7,044,680 units of Herbert Bone Screws and Cannulated Bone Screws because packaging operations at a Puerto Rico facility were not properly validated.

    Product
    HERBERT BONE SCREW, 3.0MM and HERBERT CANNULATED BONE S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1014-2014·2014-02-26

    Zimmer Recalls One-Piece Lag Screws Due to Packaging Validation Issues

    Zimmer is recalling 7,044,680 one-piece lag screws because packaging operations at its Puerto Rico facility were not properly validated, despite passing seal integrity tests.

    Product
    ONE-PIECE LAG SCREW 11MM. Item codes starting with 00225900.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V081000·2014-02-25

    NABI Recalls 2013-2014 Buses Due to Intake Manifold Freeze Risk

    NABI is recalling 269 city transit buses because condensation in the intake manifold may freeze, potentially causing exhaust flames or vehicle fire.

    Product
    NABI — NABI LFW, BRT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·14115·2014-02-25

    BRP Recalls Ski-Doo and Can-Am Heated Gloves Due to Fire Hazard

    BRP is recalling Ski-Doo and Can-Am heated gloves and lithium-ion batteries because the battery packs can overheat and cause fires. No injuries were reported, but minor property damage occurred.

    Product
    Ski-Doo® and Can-Am® heated gloves and Lithium-Ion Rechargeable Batteries.
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14114·2014-02-25

    Genie Recalls Garage Door Openers Due to Fire Hazard

    Genie is recalling specific screw drive garage door openers because the control board can overheat, posing a fire hazard. No injuries have been reported.

    Product
    Garage door openers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·14113·2014-02-25

    Rollerblade USA Recalls Tempest Inline Skates Due to Fall Hazard

    Rollerblade USA is recalling about 11,800 pairs of Tempest inline skates because misaligned mounting holes can cause the boot to separate from the frame, posing a fall hazard.

    Product
    Rollerblade® Tempest Inline Skates
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V073000·2014-02-24

    Prevost Recalls 2008-2010 X3-45 Coaches Due to Fire Risk

    Prevost is recalling 2008-2010 X3-45 coaches because a specific DC to DC converter potting compound may conduct electricity and cause a fire.

    Product
    PREVOST — PREVOST X3-45
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V082000·2014-02-21

    Kalmar Recalls 2010-2013 Ottawa Terminal Tractors Due to Fire Risk

    Kalmar is recalling certain 2010-2013 Ottawa terminal tractors because condensation in the intake manifold may freeze, causing elevated exhaust temperatures or flames that increase the risk of fire or burn injury.

    Product
    OTTAWA — OTTAWA TERMINAL TRACTOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V079000·2014-02-21

    Daimler Recalls Thomas Built Buses Due to Intake Manifold Sensor Defect

    Daimler is recalling 2009-2015 Thomas Built Saf-T-Liner HDX school buses because condensation in the intake manifold may freeze, causing sensor malfunction and increasing the risk of fire or burn injury.

    Product
    THOMAS BUILT BUSES — THOMAS BUILT BUSES SAF-T-LINER HDX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V080000·2014-02-21

    Daimler Trucks Recalls 2008-2015 Vehicles Due to Intake Manifold Defect

    Daimler Trucks North America is recalling specific 2008-2015 Freightliner, Sterling, and Thomas Built Buses vehicles because condensation in the intake manifold may freeze, causing sensor malfunction and increasing the risk of fire or burn injury.

    Product
    FREIGHTLINER — FREIGHTLINER, THOMAS BUILT BUSES, STERLING CASCADIA, M2, SAF-T-LINER HDX, LT8500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V092000·2014-02-21

    GM Recalls 2014 Vehicles for Transmission Shift Cable Defect

    General Motors is recalling 2014 Buick, Chevrolet, and GMC vehicles because the transmission shift cable may disengage, creating a risk of the vehicle rolling away.

    Product
    CHEVROLET — CHEVROLET, BUICK, GMC IMPALA, VERANO, TRAVERSE, MALIBU
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V078000·2014-02-21

    Mack Trucks Recalls 70,208 Vehicles for Electrical Fire Risk

    Mack Trucks is recalling 70,208 vehicles from model years 2007-2015 because water leaks may contaminate the Electronic Power Distribution Module, increasing the risk of a fire.

    Product
    MACK — MACK PINNACLE (CHU), GU, GRANITE (GU), PINNACLE (CXU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V088000·2014-02-21

    Mack LEU Trucks Recalled for Exhaust Pipe Disconnection Risk

    Mack is recalling 2010-2015 LEU trucks with Cummins ISL engines because the exhaust pipe may disconnect, potentially exposing operators to carbon monoxide.

    Product
    MACK — MACK LEU
    Category
    Vehicle
    Distribution
    Distributed nationwide