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.

57526–57550 of 74005

  • HighCPSC·14259·2014-08-20

    Attwood Recalls Kayak and Watersports Storage Hangers Due to Injury Hazard

    Attwood is recalling kayak and watersports storage hangers because the length adjustment buckles may release unexpectedly, causing stored items to fall and injure people nearby.

    Product
    Kayak and Watersports Storage Hanger
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2229-2014·2014-08-20

    Zimmer Recalls Nonsterile VER2 Handle Due to Assembly Failure

    Zimmer, Inc. is recalling 412 units of the VER2 Handle, Pin Rework, RT Nonsterile because the handle may fail to remain assembled to the rasp during use.

    Product
    VER2 HANDLE, PIN REWORK, RT Nonsterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2167-2014·2014-08-20

    Esaote PA230E Ultrasound Transducer Recalled for Excessive Surface Temperature

    Biosound Esaote, Inc. is recalling 1,301 PA230E ultrasound transducers because they may exceed maximum allowable surface temperature limits under specific settings.

    Product
    Esaote PA230E Transducer A portable and cart base ultrasound system for general and cardiovascular imaging
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·14V512000·2014-08-20

    Autocar Recalls 2015 Xspotter Trucks Due to Fuel Filter Defect

    Autocar is recalling 19 model year 2015 Xspotter heavy-duty trucks because a fuel filter defect may cause the engine to stall without warning, increasing the risk of a crash.

    Product
    AUTOCAR — AUTOCAR XSPOTTER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2210-2014·2014-08-20

    Medical Positioning Rapid Response HUT Table Recall for Malfunction Risk

    Medical Positioning Inc. is recalling 17 Rapid Response HUT tables because a defective component may cause the table to drop into the Trendelenburg position more rapidly than normal under excessive weight.

    Product
    Medical Positioning Rapid Response HUT table with Dual 2 Way Drop Section, Powered Medical Examination table, Model # 1217. Product Usage: Used to conduct syncope examinations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2174-2014·2014-08-20

    Siemens Linear Accelerators Recalled for Potential Patient Collision Risk

    Siemens Medical Solutions is recalling 160 linear accelerators because automatic treatment movements could cause the machine to collide with patients.

    Product
    Siemens Linear Accelerators of type ARTISTE, ONCOR, and PRIMUS with Automatic Sequenced Cancer Treatment Delivery Option.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2172-2014·2014-08-20

    Medtronic Recalls Ascenda Intrathecal Catheters Due to Retainer Ring Defect

    Medtronic is recalling specific lots of Ascenda Intrathecal Catheters and Revision Kits because a retainer ring component may not meet specifications, risking catheter disconnection.

    Product
    Medtronic Ascenda Intrathecal Catheter models 8780 and 8781, and Ascenda Intrathecal Catheter Pump Segment Revision Kit, model 8784. The Ascenda Intrathecal Catheter is part of an infusion system that stores and delivers parenteral drugs to the intrathecal space. The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2218-2014·2014-08-20

    Zimmer Recalls Double Offset Rasp Handles Due to Assembly Failure

    Zimmer, Inc. is recalling 412 Double Offset Rasp Handles because the handle may fail to remain assembled to the rasp during use.

    Product
    Double Offset Rasp Handle, Left Hand Nonsterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2223-2014·2014-08-20

    Zimmer Recalls Nonsterile Orthopedic Rasps Due to Handle Failure

    Zimmer, Inc. is recalling 412 units of nonsterile orthopedic rasps because the handle may fail to remain assembled during use.

    Product
    Vl DBL OFFST WI LRG STPL, RT Nonsterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2211-2014·2014-08-20

    Medical Positioning Rapid Response HUT Table Recalled for Malfunction Risk

    Medical Positioning Inc. is recalling Model # 1219 HUT tables because a defective component may cause the table to drop rapidly into the Trendelenburg position under excessive weight.

    Product
    Medical Positioning Rapid Response HUT table, Powered Medical Examination table, Model # 1219. Product Usage: Used to conduct syncope examinations.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-2221-2014·2014-08-20

    Zimmer Recalls Double Offset Rasp Handles Due to Assembly Failure

    Zimmer, Inc. is recalling 412 nonsterile Double Offset Rasp Handles that may fail to remain assembled during use.

    Product
    Double Offset Rasp Handle, Left Hand Nonsterile
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2215-2014·2014-08-20

    Zimmer Recalls Moore Hip Prosthesis Stems Due to Packaging Failures

    Zimmer, Inc. is voluntarily recalling 68 units of Moore Hip Prosthesis Long Fenestrated Stems because packaging design verification tests failed, allowing stems to breach package trays.

    Product
    Moore Hip Prosthesis Long Fenestrated Stem 38 mm (1-1/2 Inch) Head Diameter 203 mm Length. Product Usage: The Moore Hip Prosthesis is a femoral him stem that can be used where there is roentgenogrpahic evidence of a satisfactory actabulum and sufficient bone in the femoral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2169-2014·2014-08-20

    Abbott 5 mL Reaction Vessels Recalled for Insufficient Rim Defect

    Abbott Molecular is recalling 5 mL Reaction Vessels for the m2000sp system because an insufficient rim may cause the vessels to drop through the carrier.

    Product
    5 mL Reaction Vessels (a consumable of the Abbott m2000sp Automated Fluid Handling System). The Abbott m2000 RealTime System is intended for use in performing nucleic acid amplification testing by polymerase chain reaction in clinical laboratories. The system is comprised of the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2236-2014·2014-08-20

    Nanosphere Recalls Verigene BC-GN Test Kits Due to Missing Particles

    Nanosphere is recalling Verigene BC-GN Test Kits because some extraction trays are missing magnetic microparticles required for DNA extraction.

    Product
    Verigene BC-GN Test Kit (Catalog number 20-005-021) includes: 1) 20 Verigene BC-GN Test Cartridges. Each Test Cartridge comes preloaded with all required reaction solutions, including wash solutions, oligonucleotide probe solution and signal amplification solutions required to…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2179-2014·2014-08-20

    Medtronic MiniMed Guardian Monitor Recall for Water Resistance Issue

    Medtronic MiniMed is recalling 86 Guardian REAL-Time monitors due to a manufacturing issue that may compromise water resistance.

    Product
    Medtronic MiniMed Guardian Monitor, Model No. CSS7100, CSS7100K Product Usage: The Medtronic MiniMed model CSS7100 and CSS7100K Guardian REAL-Time monitors are used in combination with the Minilink transmitter and Sof-sensor glucose sensor for continuous monitoring of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1536-2014·2014-08-20

    Bracco Recalls E-Z-HD Barium Sulfate Due to Low Potency

    Bracco Diagnostic Inc is recalling E-Z-HD (barium sulfate) bottles because routine stability testing revealed low pH and assay results.

    Product
    E-Z-HD — E-Z-HD (BARIUM SULFATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2178-2014·2014-08-20

    Agfa Healthcare Recalls Radiographic Film Due to Fogged Sheets

    Agfa Healthcare is recalling specific lots of radiographic film because some sheets are fogged, which may affect image quality.

    Product
    Radiomat M+ NIF 14 x 17; Radiomat SG 14 x 17 NIF; RX-B 8 x 10 in./IBF-004355; Radiomat B+ NIF 14 x 17; Radiomat B+ NIF 8 x 10; Radiomat B+ NIF 9 1/2 x 9 1/2; CX Ultra UV-G Plus NIF 11 x 14; Radiomat G Plus 14 x 17 NIF Product Usage: Radiographic film is a device that…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1537-2014·2014-08-20

    Pfizer Recalls Depo-Medrol Vials Due to pH Specification Failure

    Pfizer is recalling 93,800 vials of Depo-Medrol (methylprednisolone acetate) because a stability test showed a pH level below the registered specification.

    Product
    DEPO-MEDROL — DEPO-MEDROL (METHYLPREDNISOLONE ACETATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-2120-2014·2014-08-20

    Nidek GYC-1000 Green Laser Photocoagulator Recalled for Missing Aperture Label

    Nidek Inc is recalling 567 GYC-1000 Green Laser Photocoagulator systems because the required laser aperture label was not applied to the devices.

    Product
    GYC-1000 Green Laser Photocoagulator system The Nidek Green Laser Photocoagulator Model GYC -1000 is indicated for use in ophthalmic surgical procedures, including retinal and macular photocoagulation, iridotomy and trabeculoplasty.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V508000·2014-08-19

    NABI Recalls 2014 BRT and LFW Buses Due to Fuel Filter Defect

    NABI is recalling 35 model year 2014 BRT and LFW transit buses because a fuel filter defect may cause the engine to stall without warning, increasing crash risk.

    Product
    NABI — NABI BRT, LFW
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14258·2014-08-19

    Bexco Recalls Franklin & Ben Mason Cribs Due to Fall and Entrapment Hazards

    Bexco is recalling Franklin & Ben Mason 4-in-1 Convertible Cribs because the front panel can separate from the side panels, creating a gap that poses fall and entrapment risks to children.

    Product
    Franklin & Ben Mason 4-in-1 Convertible Cribs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V510000·2014-08-19

    Blue Bird School Bus Wheelchair Lift Platform Recall

    Blue Bird is recalling certain 2007-2015 school buses because wheelchair lift platform side plates may crack, posing an injury risk to operators.

    Product
    BLUE BIRD — BLUE BIRD VISION, ALL AMERICAN, MICRO BIRD, CONVENTIONAL
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·14257·2014-08-19

    Brita Recalls Children's Water Bottles Due to Laceration Hazard

    Brita is recalling about 242,500 children's water filter bottles because the lids can break into sharp pieces, posing a laceration hazard. No injuries have been reported.

    Product
    Brita hard-sided water filter bottle for kids
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V511000·2014-08-19

    Blue Bird Recalls Non-School Buses with Cracking Wheelchair Lifts

    Blue Bird is recalling 90 non-school buses from 2007-2015 because wheelchair lift platform side plates may crack, posing an injury risk to operators.

    Product
    BLUE BIRD — BLUE BIRD ALL AMERICAN, VISION, MICRO BIRD
    Category
    Vehicle
    Distribution
    Distributed nationwide