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.

Which agencies issued them

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.

56001–56025 of 74005

  • LowFDA (Devices)·Z-0609-2015·2014-12-24

    Stryker Laparoscopic Hook Scissors Recalled Due to Sterilization Instructions

    Stryker Endoscopy is recalling 180,573 units of laparoscopic hook scissors because the instructions for use do not support specific sterilization methods.

    Product
    PKG, HOOK SCISSORS, P/N 0250080020. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0689-2015·2014-12-24

    Stryker Laparoscopic Needle Holder Recall Due to Sterilization Instructions

    Stryker Endoscopy is recalling 180,573 laparoscopic needle holders because the instructions for use do not support specific sterilization methods.

    Product
    PKG, NEEDLE HOLDER, STRIAGHT, P/N 0250080340. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0697-2015·2014-12-24

    Stryker Laparoscopic Manual Instruments Recalled for Sterilization Instructions

    Stryker Endoscopy is recalling 180,573 units of laparoscopic manual instruments because the instructions for use do not support specific sterilization methods.

    Product
    PKG, 5MM INSULATED SHAFT 45CM, FOR BIPOLAR FORCEPS, P/N 0250080370. Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0826-2015·2014-12-24

    Teleflex Recalls Weck Hemoclip Ligating Clips Due to Labeling Error

    Teleflex Medical is recalling 3,180 units of Weck Hemoclip Ligating Clips because manufacturing and expiration dates were transposed on the packaging labels.

    Product
    WECK Hemoclip¿ Traditional Medium Tantalum Ligating Clips. Weck Ligating Clips are intended for use in procedures involving vessels or anatomic structures for which the surgeon determines ligating clips are the best choice.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0763-2015·2014-12-24

    Stryker Laparoscopic Needle Nose Forceps Recalled for Sterilization Documentation Error

    Stryker Endoscopy is recalling 180,573 units of laparoscopic needle nose forceps because the instructions for use do not support specific sterilization methods.

    Product
    PKG, 3MM INSERT, NEEDLE NOSE FORCEPS, 20CM, P/N 0250282005 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0739-2015·2014-12-24

    Stryker Fundus Grasper Forceps Recalled Due to Sterilization Instructions

    Stryker Endoscopy is recalling Fundus Grasper Forceps because the instructions for use do not support specific sterilization methods.

    Product
    PKG, 5MM, 45CM, INSERT, FUNDUS GRASPER FORCEPS, P/N 0250080735 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0666-2015·2014-12-24

    Stryker Endoscopy Recalls Palpation Probes Due to Sterilization Instructions

    Stryker Endoscopy is recalling 180,573 palpation probes because the instructions for use do not support specific sterilization methods.

    Product
    PKG, PALPATION PROBE GRADUATED 5MM 45CM, P/N 0250080136 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF)…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0804-2015·2014-12-24

    AGFA Healthcare Recalls Radiomat M+ NIF Films Due to Coating Artifacts

    AGFA Healthcare is recalling 142 units of Radiomat M+ NIF films because the coating may show small bright thin lines when processed.

    Product
    Radiomat M+ NIF 14 x 17, Radiomat M+ NIF 35CM x 43CM, Radiomat M+ NIF 10 x 12, Radiomat M+ NIF 25,4CM x 30,5CM
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0304-2015·2014-12-24

    Wockhardt Recalls Metoprolol Succinate Tablets for Dissolution Failure

    Wockhardt USA is recalling specific lots of Metoprolol Succinate Extended-Release Tablets because they failed long-term stability testing for dissolution specifications.

    Product
    Wockhardt Metoprolol Succinate, Extended-Release Tablets USP, 50 mg, a)100-count HDPE bottle (NDC 64679-735-02), b) 4000-count pack (64679-735-08), Manufactured by: Wockhardt Limited, Mumbai, India Distributed by Wockhardt USA LLC. 20 Waterview Blvd. Parsippany, NJ 07054 USA…
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V814000·2014-12-23

    Caterpillar Recalls 2015 CT660 and CT681 Trucks for Brake Fire Risk

    Caterpillar is recalling 57 model year 2015 CT660 and CT681 trucks because an improperly seated brake diaphragm may cause brake drag and a wheel end fire.

    Product
    CATERPILLAR — CATERPILLAR CT660, CT681
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V812000·2014-12-23

    Spartan Recalls 2013-2015 Motorhomes Due to Steering Linkage Defect

    Spartan Motors is recalling 277 model year 2013-2015 motorhomes and chassis cabs because steering linkage castle nuts may loosen, potentially causing a loss of steering control.

    Product
    SPARTAN — SPARTAN MM, METROSTAR, K2, GLADIATOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15054·2014-12-23

    Keurig Recalls MINI Plus Brewing Systems Due to Burn Hazard

    Keurig is recalling MINI Plus Brewing Systems because water can overheat and spray out, causing burns. Consumers should contact Keurig for a free repair.

    Product
    Keurig® MINI Plus Brewing Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V813000·2014-12-23

    Elgin Recalls 2014 Street Sweepers Due to Electrical Fire Risk

    Elgin is recalling 2014 Eagle and Road Wizard street sweepers because battery and alternator wiring may conduct excessive current, increasing the risk of a fire.

    Product
    ELGIN — ELGIN ROAD WIZARD, EAGLE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V811000·2014-12-22

    Suzuki Recalls Kizashi and SX4 Models for Shift Selector Defect

    Suzuki is recalling 2010-2013 Kizashi and SX4 vehicles because the shift selector can move out of Park without the brake pedal being depressed, increasing crash risk.

    Product
    SUZUKI — SUZUKI KIZASHI, SX4
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14E085000·2014-12-22

    Roadhouse Recalls Voss 888CF Motorcycle Helmets for Shell Defect

    Roadhouse Distribution is recalling Voss 888CF motorcycle helmets because the shell material failed penetration testing, increasing injury risk in crashes.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14E086000·2014-12-22

    Shark Recalls Certain RAW Motorcycle Helmets for Impact Failure

    Shark is recalling specific RAW motorcycle helmets that failed federal impact attenuation tests, increasing the risk of injury in a crash.

    Product
    EQUIPMENT:MOTORCYCLE:HELMETS recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14E084000·2014-12-19

    ZF Group Recalls 9-Speed Automatic Transmissions Due to Parking Pawl Defect

    ZF Group is recalling 9-speed automatic transmissions where a contaminated parking pawl may dislodge, preventing the vehicle from locking in Park and increasing crash risk.

    Product
    POWER TRAIN:AUTOMATIC TRANSMISSION recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V803000·2014-12-19

    Nissan Recalls 2015 Armada Vehicles for Transmission Parking Defect

    Nissan is recalling 2015 Armada vehicles because a transmission defect may prevent the parking pawl from fully engaging, allowing the vehicle to move while in Park.

    Product
    NISSAN — NISSAN ARMADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V805000·2014-12-19

    ARBOC Transit Buses Recalled for Electrical Fire Risk

    ARBOC is recalling 2015 Spirit of Mobility and Freedom buses because exterior electrical connections may not be weatherized, increasing fire risk.

    Product
    ARBOC — ARBOC SPIRIT OF FREEDOM, SPIRIT OF MOBILITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V804000·2014-12-19

    GM Recalls 2015 Cadillac SRX for Front Seat Track Bracket Defect

    General Motors is recalling 2015 Cadillac SRX vehicles because the front driver's seat track bracket may be incorrect, potentially causing the seat to detach during a crash.

    Product
    CADILLAC — CADILLAC SRX
    Category
    Vehicle
    Distribution
    Distributed nationwide