The Recall Desk

State

US Virgin Islands product recalls

73,598 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 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29876–29900 of 73776

  • ModerateFDA (Devices)·Z-1321-2020·2020-02-26

    Nobel Biocare Implant Retrieval Instruments Recalled for Sterility Concerns

    Nobel Biocare is recalling 11 units of Implant Retrieval Instrument Tri Channel 6.0 22 mm because a packaging sealing issue may compromise sterility.

    Product
    Implant Retrieval Instrument Tri Channel 6.0 22 mm - Product Usage: They can be used to remove implants, if the implant connection has been damaged. It can be used to remove implants with internal conical connection, internal tri-channel connection or external hex connection.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1230-2020·2020-02-26

    Siemens ADVIA Chemistry Enzymatic Creatinine Reagent Recalled for Interference

    Siemens Healthcare Diagnostics is recalling ADVIA Chemistry Enzymatic Creatinine reagent because phenindione therapy can cause falsely depressed results.

    Product
    ADVIA Chemistry Enzymatic Creatinine (ECRE_2) reagent, SMN 10335869
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1252-2020·2020-02-26

    Arrow Epidural Needle Kit Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 180 units of the Arrow EPIDURAL NEEDLE KIT SL-05500 because the product lidstock contains the incorrect expiration date.

    Product
    Arrow EPIDURAL NEEDLE KIT SL-05500
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0851-2020·2020-02-26

    Teva Recalls Tramadol Tablets Due to Incorrect Package Insert Labeling

    Teva Pharmaceuticals is recalling Tramadol Hydrochloride 50 mg tablets because the patient leaflets contain incorrect dosing instructions for unscored tablets.

    Product
    Tramadol Hydrochloride Tablets USP CIV, 50 mg, packaged in a) 100-count bottles (NDC 0093-0058-01), b) 500-count bottles (NDC 0093-0058-05), RX only, Manufactured in Czech Republic for: Teva Pharmaceuticals USA, Inc., North Wales, PA 19545
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1326-2020·2020-02-26

    Theralase Inc. Recalls TLC-2000 Therapeutic Medical Laser Systems

    Theralase Inc. is recalling 76 TLC-2000 laser systems because they were shipped with an incorrect power supply model.

    Product
    TLC-2000 Therapeutic Medical Laser System - Product Usage: Indicated for the temporary relief of knee pain.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1255-2020·2020-02-26

    Arrow PICC Kit Recalled for Incorrect Expiration Date on Lidstock

    Arrow International is recalling specific lots of PICC kits because the lidstock displays the wrong expiration date.

    Product
    Arrow Pressure Injectable Two-Lumen PICC Kit 5 Fr. x 50 cm EU-05052-HPMSB
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0844-2020·2020-02-26

    Memantine Hydrochloride Extended-Release Capsules Recalled for Dissolution Failure

    The Harvard Drug Group is recalling 246 cartons of Memantine Hydrochloride Extended-Release Capsules, 28mg, due to failed dissolution specifications observed during stability studies.

    Product
    MEMANTINE HYDROCHLORIDE — MEMANTINE HYDROCHLORIDE (MEMANTINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1239-2020·2020-02-26

    Arrow FlexTip Plus Catheterization Kit Recalled for Incorrect Expiration Date

    Arrow International Inc. is recalling 1,150 units of FlexTip Plus Combined Spinal Epidural Catheterization Kits because the product lidstock contains the incorrect expiration date.

    Product
    Arrow FlexTip Plus(R) Combined Spinal Epidural Catheterization Kit ASK-05560-WH
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1244-2020·2020-02-26

    Arrow Epidural Needle Component Recalled for Incorrect Expiration Date

    Arrow International Inc is recalling 1,839 units of Arrow Epidural Needle Component AN-05505 because the product lidstock contains the incorrect expiration date.

    Product
    Arrow EPIDURAL NEEDLE COMPONENT AN-05505
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1241-2020·2020-02-26

    Arrow StimuCath Continuous Nerve Block Kit Recalled for Incorrect Expiration Date

    Arrow International Inc is recalling 155 units of the StimuCath Continuous Nerve Block Kit because the product lidstock contains an incorrect expiration date.

    Product
    Arrow StimuCath(R) Continuous Nerve Block Kit ASK-05060-CHO1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V109000·2020-02-25

    Mercedes-Benz Sprinter Recall for Steering Spindle Bearing Screw Defect

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because steering spindle screws may loosen, increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, FREIGHTLINER SPRINTER 1500, SPRINTER 2500, SPRINTER 4500, SPRINTER 3500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V105000·2020-02-25

    Keystone Recalls 2020 Trailers Due to Spare Tire Carrier U-Bolt Failure

    Keystone RV Company is recalling 2020 Crossroads Zinger, Hideout, and Springdale trailers because spare tire carrier U-bolts may fail, allowing the carrier and tire to detach.

    Product
    KEYSTONE — KEYSTONE CROSSROADS ZINGER, HIDEOUT, SPRINGDALE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V110000·2020-02-25

    2019 Mercedes-Benz Sprinter Recall for Missing Steering Column Cover

    Daimler Vans USA is recalling 2019 Mercedes-Benz and Freightliner Sprinter vans because the steering column casing cover may be missing, potentially allowing debris to interfere with steering.

    Product
    FREIGHTLINER — FREIGHTLINER, MERCEDES-BENZ SPRINTER 2500, SPRINTER 1500, SPRINTER 3500, SPRINTER 4500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V107000·2020-02-24

    Smart Fortwo Electric Drive Recalled for Battery Fire Risk

    Mercedes-Benz is recalling one 2019 Smart Fortwo Electric Drive because a battery weld may detach, causing sudden failure, stalling, or fire.

    Product
    SMART — SMART FORTWO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V104000·2020-02-24

    HME Recalls 2016-2020 Emergency Vehicles Due to Fuse Box Seal Defect

    HME is recalling 2016-2020 AF1, 1871, and SFO emergency vehicles because a missing O-ring seal may allow moisture into the fuse box, potentially causing overheating or malfunction.

    Product
    HME — HME SFO, AF1, 1871
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V099000·2020-02-21

    2021 Ford E-350 Recalled for Rear Axle Differential Fluid Deficiency

    The 2021 Ford E-350 may have inadequate rear axle differential fluid, risking driveshaft separation and loss of drive. Ford will inspect and adjust or replace the rear axle assembly at no cost.

    Product
    FORD — FORD F-550, E-450, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide