The Recall Desk

State

US Virgin Islands product recalls

73,388 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
177
Critical
12
Severe
39
Most recent
2026-09-23

Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,388 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

21076–21100 of 73565

  • HighFDA (Devices)·Z-0905-2022·2022-04-20

    Breast Milk Analyzer Lacks FDA Validation, Risks Sub-optimal Infant Nutrition

    Stanbio Laboratory's Creamatocrit Plus breast milk analyzer was marketed without required FDA 510(k) clearance. Its performance has not been validated, and erroneous results could lead to inadequate nutritional supplementation for infants.

    Product
    Separation Technology Creamatocrit Plus, Catalog Number: 100-146
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0942-2022·2022-04-20

    ARIA Radiation Therapy Management Software May Cause Treatment Location Error

    Varian ARIA radiation therapy management software versions 13.6 through 16.1 may generate incorrect treatment plan values that could direct radiation therapy to the wrong location. No illnesses have been reported.

    Product
    ARIA Radiation Therapy Management (RTM) VERSIONS 13.6, 15.1, 15.5, 15.6, 16.0, 16.1
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0938-2022·2022-04-20

    Pre-wired ECG Electrode Set Fails Defibrillation Voltage Safety Standard

    Graphic Controls' CLARAVUE Pre-wired Electrode set does not meet required electrical specifications for defibrillation use. The device fails to withstand 5,000 volts without breakdown, potentially resulting in ineffective defibrillation.

    Product
    CLARAVUE Pre-wired Electrode - IP SET 12 RT ADULT-US Model: 32028779 50602-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0925-2022·2022-04-20

    Abbott Vascular Plus 30 Priority Pack Recalled for Connection Leaks

    Abbott Vascular is recalling seven lots of the Plus 30 Priority Pack due to increased reports of leaks and intermittent loose connections in the vascular devices.

    Product
    Plus 30 Priority Pack w/.096 RHV - REF 1000183 WPL2122277-01 (20-03-01) Plus 30 Priority Pack w/.115 RHV - REF 1000185-115 WPL2122279-01 (2019-03-01)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0913-2022·2022-04-20

    Hammertoe Correction Surgical System Recalled for Driver Connection Defect

    Nextremity Solutions recalls the Nextra Hammertoe Correction System because the driver's proximal end is oversized, making it difficult to connect and remove from the implant, potentially delaying surgery.

    Product
    Nextra Hammertoe Correction System 3.5 Middle and 3.2 Proximal Saw Cut SKU: NX-3532K-SC Orthopedic surgical instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0989-2022·2022-04-20

    Cinnamon Crumb Cake Recalled for Potential Foreign Materials

    Continental Mills voluntarily recalls Krusteaz Cinnamon Crumb Cake (Lot KX2063) due to potential foreign materials that could pose a choking or injury risk.

    Product
    Item # 722-0105, Krusteaz Cinnamon Crumb Cake. Product is shelf stable and packaged in a box. net wt. 21 oz., UPC 0 41449 11140 7.
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0937-2022·2022-04-20

    CLARAVUE Pre-wired Electrode fails to meet electrical safety specification

    Graphic Controls' CLARAVUE Pre-wired Electrode units fail to meet electrical safety specifications required for defibrillation. The device delivers an inefficient electrical charge and may result in ineffective defibrillation.

    Product
    CLARAVUE Pre-wired Electrode - IP SET M5 RT ADULT-US Model: 32028778 50601-US
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0929-2022·2022-04-20

    Siemens Atellica CH Hemoglobin A1c Reagent Kits Recalled for Quality Control Issues

    Siemens Healthcare is recalling Atellica CH Hemoglobin A1c reagent kits due to potential reagent carryover affecting quality control and patient test results. The issue may cause inaccurate diabetes monitoring measurements.

    Product
    Atellica CH Enzymatic Hemoglobin A1c (A1c_E/A1c_H), Siemens Material Number 11097536
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0911-2022·2022-04-20

    Nextra Hammertoe Correction System surgical instruments recalled for defective connector

    Nextremity Solutions recalls 459 units of the Nextra Hammertoe Correction System due to an oversized proximal driver end that prevents proper connection and removal during surgery.

    Product
    Nextra Hammertoe Correction System 4.5 Middle and 3.2 Proximal Saw Cut SKU: NX-4532K-SC Orthopedic surgical instrument
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0984-2022·2022-04-20

    Great Value Buttermilk Pancake Mix Recalled for Foreign Materials

    Continental Mills is recalling Great Value Buttermilk Pancake & Waffle Mix (item #714-5000) due to foreign materials. Approximately 1,125 cases were distributed nationwide.

    Product
    Item # 714-5000, Great Value Buttermilk Pancake & Waffle Mix. Product is shelf stable and packaged in a box. net wt. 32 oz., UPC 0 78742 37082 8.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0766-2022·2022-04-20

    Cyanocobalamin Injection Recalled for Subpotent Drug - Out of Specification Assay

    Aurobindo Pharma USA Inc. is recalling 433,809 vials of Cyanocobalamin injection nationwide because assay testing showed the drug is subpotent, containing less than the specified 1,000 mcg/mL of active ingredient. Affected lots with specific expiration dates from September 2022 to April 2023 are identified for recall.

    Product
    CYANOCOBALAMIN — CYANOCOBALAMIN (CYANOCOBALAMIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0926-2022·2022-04-20

    Philips Autoclavable Temperature Probes: Updated Cleaning Instructions

    Philips is updating instructions for cleaning and disinfecting reusable autoclavable temperature probes due to revisions needed in the disinfection process.

    Product
    The IFU for the Autoclavable Temperature Probes: Part # 453564635891, providing in the packaging for the following product model #s: 21075A, 21076A, 21078A, 989803162621, 989803162631, 989803162641.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Food)·F-0988-2022·2022-04-20

    Krusteaz Belgian Waffle Mix recalled due to foreign materials contamination

    Continental Mills voluntarily recalled 450 cases of Krusteaz Belgian Waffle Mix nationwide due to the presence of foreign materials.

    Product
    Item # 721-1000, Krusteaz Belgian Waffle Mix. Product is shelf stable and packaged in a box. net wt. 28 oz., UPC 0 41449 00186 9.
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0930-2022·2022-04-20

    Siemens Atellica CH Fructosamine Reagent Recalled for Potential Carryover

    Siemens Healthcare Diagnostics is recalling Atellica CH Fructosamine reagent (lots 211359, 211451) due to potential reagent carryover that could affect diagnostic test accuracy.

    Product
    Atellica CH Fructosamine (Fruc), Siemens Material Number 11097637
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·22E034000·2022-04-19

    Enerco Recalls LP Gas Quick Connector Fittings for Fire Risk

    Enerco is recalling specific Mr. Heater LP gas quick connector fittings because they may crack and leak gas, increasing the risk of fire.

    Product
    EQUIPMENT:RECREATIONAL VEHICLE/TRAILER:LPG SYSTEMS:LINES AND FITTINGS recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V265000·2022-04-19

    Maserati Recalls 2022 MC20 Vehicles Due to Brake Light Malfunction

    Maserati is recalling 2022 MC20 vehicles because faulty rear tail lights may cause brake lights to flicker, potentially confusing other drivers and increasing crash risk.

    Product
    MASERATI — MASERATI MC20
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateNHTSA·22V266000·2022-04-19

    Triple E RV Recalls 2021-2022 Wonder W24RL for Incorrect Weight Decal

    Triple E Recreational Vehicles is recalling 2021-2022 Wonder W24RL models because an incorrect weight decal may lead to overloading the storage compartment.

    Product
    TRIPLE E RV — TRIPLE E RV WONDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V264000·2022-04-18

    2022 Tesla Model X: Missing Seat Reinforcement Bracket Safety Defect

    Tesla is recalling one 2022 Model X vehicle due to a missing body structure reinforcement bracket at the second-row seat. This failure to comply with federal seat restraint standards increases the risk of occupant injury in a crash.

    Product
    TESLA — TESLA MODEL X
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V263000·2022-04-18

    Tesla Model 3 Speedometer Unit Display May Fail in Track Mode

    Tesla is recalling certain 2018-2022 Model 3 Performance vehicles because the speedometer's mph/km/h unit display may fail in Track Mode. Drivers may not know their vehicle's speed, increasing crash risk. Tesla will provide a free software update.

    Product
    TESLA — TESLA MODEL 3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·009-2022·2022-04-16

    Firehouse Jams Recalls Uncured Bacon Marmalade Produced Without Inspection

    Firehouse Jams is recalling 3,819 pounds of uncured bacon marmalade produced without federal inspection. No adverse reactions have been reported.

    Product
    Firehouse Jams, LLC Recalls Uncured Bacon Marmalade Products Produced Without Benefit of Inspection
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V260000·2022-04-15

    Rugged Mountain Custom RV Travel Trailer Recall for Coupler Welding Defect

    Tiny Idahomes is recalling 2021-2022 Rugged Mountain Custom RV Travel trailers because an improperly welded coupler may cause the trailer to separate from the tow vehicle.

    Product
    RUGGED MOUNTAIN CUSTOM RV — RUGGED MOUNTAIN CUSTOM RV TRAVEL TRAILER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V262000·2022-04-15

    2019-2021 Autocar Xpeditor Vehicles Recall: Inoperable Hazard Lights

    Autocar is recalling 2019-2021 Xpeditor vehicles because the hazard lights do not function when the ignition is off, increasing crash risk. Dealers will repair or replace the wire harness at no charge.

    Product
    AUTOCAR — AUTOCAR XPEDITOR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·22V261000·2022-04-15

    2021 Mercedes-Benz AMG GLC63 S Headlight Failure Recall

    Mercedes-Benz is recalling certain 2021 GLC models because the headlight electrical connection may not be watertight, risking headlight failure. Reduced visibility increases crash risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG GLC63 S, AMG GLC63, AMG GLC43, GLC 300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·22V246000·2022-04-14

    GM Recalls 2015 Enclave, Traverse, Acadia for Air Bag Defect

    General Motors is recalling 2015 Buick Enclave, Chevrolet Traverse, and GMC Acadia vehicles because the driver's air bag inflator may explode during deployment.

    Product
    GMC — GMC, BUICK, CHEVROLET ACADIA, ENCLAVE, TRAVERSE
    Category
    Vehicle
    Distribution
    Distributed nationwide