The Recall Desk

State

US Virgin Islands product recalls

73,566 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 73,566 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

26676–26700 of 73744

  • ModerateFDA (Food)·F-0157-2021·2020-12-16

    Chef Myron's Tsukeyaki Sauce Recalled for Gluten-Free Labeling Error

    JMH International is recalling Chef Myron's Tsukeyaki Sauce because it contains wheat-derived ingredients despite a gluten-free claim.

    Product
    Chef Myron's Tsukeyaki Sauce, 64 FL OZ (1.89 L), Item # 400023276, 4 bottles/case
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0546-2021·2020-12-16

    Randox Mg R1 Magnesium Test Kit Recalled for Linearity Performance Failure

    Randox Laboratories is recalling Randox Mg R1 kits due to reduced linearity performance, which may affect the accuracy of magnesium test results.

    Product
    Randox Mg R1 - Product Usage: For the quantitative in vitro determination of Magnesium in serum, plasma and urine Catalogue Number: MG3880
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0536-2021·2020-12-16

    Chromsystems 3PLUS1 Multilevel Plasma Calibrator Set Recalled for Stability Issues

    Chromsystems is recalling 3PLUS1 Multilevel Plasma Calibrator Sets because they do not meet stability criteria, which may impact test results.

    Product
    3PLUS1 Multilevel Plasma Calibrator Set, Order No. 75128 - Product Usage: The kit is intended for amino acid metabolic screening, confirmation of a tentative diagnosis, and monitoring of treatment in individuals diagnosed with a metabolic disorder.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0548-2021·2020-12-16

    Integra Recalls Mayfield A2000 Skull Cap Instruction Manual

    Integra LifeSciences Corp. is recalling 552 instruction manuals for the Mayfield A2000 Skull Cap to correct inaccurate illustrations.

    Product
    Instruction Manual for Mayfield A2000 Skull Cap - Product Usage: intended for or rigid skeletal fixation during neurosurgical procedures. P/N: 451A2000
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0562-2021·2020-12-16

    BD Multi-Check CD4 Low Control Recalled for Inaccurate Flow Cytometry Results

    Becton, Dickinson and Company is recalling 619 vials of BD Multi-Check CD4 Low Control due to unexpected cell populations that may cause inaccurate flow cytometry results.

    Product
    BD" Multi-Check CD4 Low Control 2.5 mL IVD - Product Usage: intended as a complete process control for immunophenotyping by flow cytometry.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0553-2021·2020-12-16

    Welch Allyn ELI 380 Electrocardiograph Recalled for Wireless Disconnection

    Welch Allyn is recalling 1,009 ELI 380 Electrocardiographs because the internal radio can disconnect from the wireless access point.

    Product
    ELI 380 Electrocardiograph - Product Usage: intended to be a high-performance, multichannel resting electrocardiograph. As a resting electrocardiograph, the ELI 380 simultaneously acquires data from each lead.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0152-2021·2020-12-16

    Chef Myron's Eurasian Fusion Sauce Recalled for Gluten Mislabeling

    JMH International is recalling Chef Myron's Eurasian Fusion Sauce because it contains wheat-derived fermented soy sauce despite a gluten-free claim.

    Product
    Chef Myron's Eurasian Fusion Sauce, 64 FL OZ (1.89 L), Item # 400023288, 4 bottles/case.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0549-2021·2020-12-16

    Canon CT Scanner Recall for Software Issue Causing Scan Failures

    Canon Medical System is recalling 60 Aquilion Prime SP CT scanners due to a software defect that may prevent automatic scans, requiring rescans and contrast reinjection.

    Product
    Canon Aquilion Prime SP, Multislice Helical CT Scanner, TSX-303B/8L - Product Usage: intended to acquire and display cross-sectional volumes of the whole body, including the head.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0563-2021·2020-12-16

    Spacelabs Sentinel V10 and V11 Software Upgrade Recall

    Spacelabs Healthcare is recalling Sentinel V10.x and V11.x software because system upgrades may add or overwrite unrelated comments on existing ECG and ABP tests.

    Product
    Sentinel V10.x & V11.x, Models: 98200 & 98201 - Product Usage: designed using the latest programming technology and is easy to install and to use.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0158-2021·2020-12-16

    Chef Myron's Yakitori Sauce Recalled for Gluten-Free Labeling Error

    JMH International is recalling Chef Myron's Yakitori Sauce because it contains wheat-derived ingredients despite a gluten-free claim.

    Product
    Chef Myron's Yakitori Sauce, 64 FL OZ (1.89 L), Item # 400023316, 4 bottles/case
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0156-2021·2020-12-16

    Chef Myron's Tangy Teriyaki Sauce Recalled for Gluten Mislabeling

    JMH International is recalling Chef Myron's Tangy Teriyaki Sauce because it contains wheat-derived ingredients despite a gluten-free claim.

    Product
    Chef Myron's Tangy Teriyaki Sauce, 64 FL OZ (1.89 L), Item # 400023221, 4 bottles/case
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0538-2021·2020-12-16

    Chromsystems Recalls MassChrom Amino Acid Analysis Plasma Control Level II

    Chromsystems Instruments & Chemicals GmbH is voluntarily recalling 363 vials of MassChrom Amino Acid Analysis Plasma Control Level II due to a Class II device defect.

    Product
    MassChrom Amino Acid Analysis Plasma Control Level II, Order No. 0472 - Product Usage: The kit is intended for amino acid metabolic screening, confirmation of a tentative diagnosis, and monitoring of treatment in individuals diagnosed with a metabolic disorder.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-0127-2021·2020-12-16

    Novocol Recalls Scandonest 3% Plain Due to Labeling Mix-Up

    Novocol Pharmaceutical is recalling 15,398 cartridges of Scandonest 3% Plain (Mepivacaine Hydrochloride) due to a label mix-up. The product is distributed nationwide.

    Product
    SCANDONEST 3% PLAIN — SCANDONEST 3% PLAIN (MEPIVACAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V782000·2020-12-15

    2021 Volvo Truck Air Brake Line Defect Recall

    Volvo Trucks is recalling 6,982 commercial trucks (2021 VHD, VNL, VNR, and VAH models) because damaged collets in the air brake system may cause park brakes to apply unexpectedly, potentially causing loss of vehicle control.

    Product
    VOLVO — VOLVO VAH, VNL, VHD, VNR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V780000·2020-12-15

    Certain Jayco and Entegra Motorhomes Leveling System Support Bracket Defect Recall

    Jayco and Entegra are recalling certain 2020-2021 motorhomes with defective leveling system support brackets that may fail, allowing components to contact the ground and potentially leak hydraulic fluid, increasing crash risk.

    Product
    JAYCO — JAYCO, ENTEGRA REDHAWK SE, ESTEEM, GREYHAWK, REDHAWK
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V781000·2020-12-15

    Ducati Scrambler motorcycles recalled due to electrical short-circuit fire risk

    Certain 2018-2021 Ducati Scrambler 1100 motorcycles may experience an electrical short-circuit when the exhaust valve cable contacts the positive battery wire, increasing fire risk. Dealers will install a new cable guide and cable tie at no charge.

    Product
    DUCATI — DUCATI SCRAMBLER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V783000·2020-12-15

    AEV Ambulances Recalled for Potential LCD Display Malfunction

    Halcore is recalling specific 2020-2021 AEV ambulances because electrical spikes may cause the emergency lighting and HVAC control display to lock up or fail.

    Product
    AEV — AEV TYPE 1 F-SERIES AMBULANCE, TRAUMAHAWK, FREIGHTLINER M2 AMBULANCE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V779000·2020-12-15

    Rosenbauer Emergency Vehicles Recalled for LCD Display Lockup Defect

    Rosenbauer America is recalling specific emergency vehicles because LCD displays may lock up due to voltage spikes, potentially delaying emergency efforts.

    Product
    ROSENBAUER — ROSENBAUER COMMANDER, AVENGER, WARRIOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V774000·2020-12-11

    Kawasaki Recalls 2021 Ninja 400 and Z400 Motorcycles for Engine Defect

    Kawasaki is recalling 2021 Ninja 400 and Z400 motorcycles because a weak camshaft chain tensioner could cause the engine to stall, increasing crash risk.

    Product
    KAWASAKI — KAWASAKI NINJA 400, EX400G, Z400
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V772000·2020-12-11

    Mercedes-Benz Recalls One 2019 Sprinter 2500 for Hood Installation Defect

    Daimler Vans USA is recalling one 2019 Mercedes-Benz Sprinter 2500 because the engine hood may not have been installed properly, posing an injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ SPRINTER 2500
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20E091000·2020-12-11

    Ohlins Recalls Front Struts for Porsche 911 Models Due to Pin Breakage Risk

    Ohlins is recalling front struts for specific Porsche 911 models because the strut pin may break during maximum steering, potentially causing loss of vehicle control.

    Product
    PORSCHE — PORSCHE 911 CARRERA, 911 TURBO
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V776000·2020-12-11

    Mercedes-Benz Recalls AMG GLC63 Vehicles Due to Starter Cable Defect

    Mercedes-Benz is recalling 2,563 AMG GLC63 vehicles because a starter cable may chafe and short-circuit, increasing the risk of a stall or fire.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLC63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V775000·2020-12-11

    Mercedes-Benz Recalls 2020 AMG GT Vehicles for Headlight Aim Defect

    Mercedes-Benz is recalling 2020 AMG GT vehicles because headlights may be aimed too high, reducing visibility of oncoming traffic and increasing crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GT
    Category
    Vehicle
    Distribution
    Distributed nationwide