The Recall Desk

State

US Virgin Islands product recalls

73,737 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 73,737 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

35876–35900 of 73915

  • HighFDA (Devices)·Z-0522-2019·2018-12-05

    GE Healthcare Recalls Solar 8000i Patient Monitoring Systems

    GE Healthcare is recalling approximately 73,673 Solar 8000i and 8000M patient monitoring systems because they may simultaneously restart during prolonged network overloads.

    Product
    Solar 8000i Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0518-2019·2018-12-05

    Fresenius Granuflo Dry Acid Concentrate Recalled for Foreign Substance

    Fresenius Medical Care is recalling Granuflo Dry Acid Concentrate for hemodialysis due to confirmed foreign substance contamination.

    Product
    Fresenius Granuflo Dry Acid Concentrate- 3K 2.5 Ca 1 Mg 16.5 GAL Catalog Number: OFD3251-3B for hemodialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0501-2019·2018-12-05

    NxStage PureFlow B Solution Recalled Due to Bag Burst Risk

    NxStage Medical is recalling PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may injure eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-401, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0677-2019·2018-12-05

    Duncan Hines Confetti Cake Mix Recalled for Salmonella

    ConAgra Foods is recalling Duncan Hines Signature Confetti Cake Mix after a positive finding of Salmonella in a retail sample.

    Product
    Duncan Hines Signature Confetti Cake cake mix 15.25oz. 12 retail units per case 644209414550
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0676-2019·2018-12-05

    Duncan Hines Cake Mix Recalled for Salmonella Contamination

    ConAgra Foods is recalling Duncan Hines Classic Butter Golden cake mix due to a positive Salmonella finding in a retail sample.

    Product
    Duncan Hines Classic Butter Golden cake mix 15.25oz. 12 retail units per case 644209307593
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0515-2019·2018-12-05

    Eurotrol HemoTrol Level 3 Recalled Due to Microbial Contamination

    Eurotrol Inc. is recalling HemoTrol Level 3 hematology quality control mixtures because microbial contamination causes incorrect, lower-than-assigned measurement results.

    Product
    HemoTrol Level 3- In Vitro Diagnostic Hematology quality control mixture. Catalogue number: 171.003.002 Eurotrol HemoLin is an assayed hemoglobin control intended for professional use in the verification of the linearity of the HemoCue¿ Hb 201 systems.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0674-2019·2018-12-05

    Duncan Hines Classic White Cake Mix Recalled for Salmonella

    ConAgra Foods is recalling Duncan Hines Classic White cake mix after a positive finding of Salmonella in a retail sample.

    Product
    Duncan Hines Classic Classic White cake mix 15.25oz. 12 retail units per case 644209307500
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0520-2019·2018-12-05

    GE Healthcare Recalls Dash 4000 Patient Monitoring Systems

    GE Healthcare is recalling Dash 4000 Patient Monitoring Systems because they may simultaneously restart if connected to the same network during a prolonged network overload.

    Product
    Dash 4000 Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0504-2019·2018-12-05

    NxStage PureFlow B Solution Recalled for Potential Bag Burst Injury Risk

    NxStage Medical is recalling PureFlow B Solution because the smaller chamber of the two-chamber bag can burst, releasing electrolyte fluid that may cause injury if it contacts eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-404, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0500-2019·2018-12-05

    NxStage PureFlow B Solution Recalled for Potential Bag Bursting

    NxStage Medical is recalling 59,100 units of PureFlow B Solution because the smaller chamber may burst, releasing electrolyte fluid that can injure eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-400, Premixed Dialysate for Hemodialysis. NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0675-2019·2018-12-05

    Duncan Hines Classic Yellow Cake Mix Recalled for Salmonella

    ConAgra Foods is recalling Duncan Hines Classic Yellow cake mix after a positive finding of Salmonella in a retail sample.

    Product
    Duncan Hines Classic Classic Yellow cake mix 15.25oz. 12 retail units per case 644209307494
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-0503-2019·2018-12-05

    NxStage PureFlow B Solution Recalled Due to Bag Burst Risk

    NxStage Medical is recalling 2,189 units of PureFlow B Solution because the bag's smaller chamber can burst, releasing electrolyte fluid that may injure eyes or skin.

    Product
    NxStage PureFlow B Solution-RFP-403, Premixed Dialysate for Hemodialysis NxStage PureFlow B Solution is indicated for use with renal replacement therapy systems that utilize sterile premixed dialysate during hemodialysis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·18V865000·2018-12-05

    Elgin Street Sweepers Recalled for Air Brake Fitting Failure Risk

    Elgin is recalling 2015-2018 street sweepers because a T-fitting on the air brake system may fail, causing the parking brake to apply unexpectedly and increasing crash risk.

    Product
    ELGIN — ELGIN BROOM BEAR, WHIRLWIND, EAGLE, ROAD WIZARD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0517-2019·2018-12-05

    Fresenius Granuflo Dry Acid Concentrate Recalled for Foreign Substance

    Fresenius Medical Care is recalling specific lots of Granuflo Dry Acid Concentrate for hemodialysis due to the presence of a foreign substance.

    Product
    Fresenius Granuflo Dry Acid Concentrate- 2K 2.5 Ca 1 Mg 16.5 GAL Catalog Number: OFD2251-3B for hemodialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0519-2019·2018-12-05

    GE Healthcare Recalls Dash 3000 Patient Monitoring Systems

    GE Healthcare is recalling Dash 3000 patient monitors because they may restart simultaneously during prolonged network overloads.

    Product
    Dash 3000 Patient Monitoring System is used to monitor physiologic parameter data on adult, pediatric and neonatal patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0498-2019·2018-12-05

    Stryker Recalls Reprocessed Xcel Bladeless Trocars Due to Distribution Error

    Stryker Sustainability Solutions is recalling 4,848 reprocessed Xcel Bladeless Trocars (H12LP) because they were distributed to facilities after a previous recall was executed.

    Product
    Reprocessed Xcel Bladeless Trocar (H12LP) Model # H12LP Reprocessed Endoscopic Trocars12x100mm - Product Usage: Physical Product Description: The Reprocessed Blunt Tip Trocar consists of a radiolucent cannula and obturator sized 12mm in diameter (refer to Figure 1). The…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1208-2019·2018-12-05

    Akorn Recalls Clindamycin Phosphate Topical Solution Due to Impurity Failures

    Akorn, Inc. is recalling 58,393 jars of Clindamycin Phosphate Topical Solution USP, 1% because the product failed impurity and degradation specifications.

    Product
    Clindamycin Phosphate Topical Solution USP, 1% (10 mg/mL clindamycin), 60 pledget applicators per jar, Rx only. Manufactured by Ei LLC 2865 N. Cannon Blvd. Kannapolis, NC 18083. NDC# 61748-0201-60
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0509-2019·2018-12-05

    Tosoh AIA-900 Analyzer Recalled for Potential Drive Motor Failure

    Tosoh Bioscience is recalling 247 AIA-900 Automated Immunoassay Analyzers due to a potential drive motor defect that may cause the device to stop functioning and delay patient test results.

    Product
    AIA-900 Automated Immunoassay Analyzer, product code 022930 /022930R Product Usage: The AIA-900 is capable of performing three methods of immunoassay: an immunoenzymetric (IEMA) or sandwich immunoassay, a competitive binding (EIA) immunoassay, and a two-step immunoenzymetric…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-0499-2019·2018-12-05

    Siemens Dimension Vista Lactate Dehydrogenase Reagent Cartridge Recall

    Siemens is recalling Dimension Vista Lactate Dehydrogenase reagent cartridges because they may produce falsely elevated results if used after Lactic Acid assays.

    Product
    Dimension Vista Lactate Dehydrogenase (LDI) Flex reagent cartridge, an in vitro diagnostic test for the quantitative measurement of lactate dehydrogenase in human serum and plasma on the Dimension Vista¿ System.Cat. No. K2054, Mat. No. 10464323
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-0516-2019·2018-12-05

    Fresenius Granuflo Dry Acid Concentrate Recalled for Foreign Substance

    Fresenius Medical Care is recalling Granuflo Dry Acid Concentrate for hemodialysis due to confirmed foreign substance contamination.

    Product
    Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg 16.5 GAL Catalog Number: OFD2201-3B for hemodialysis
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V859000·2018-12-04

    Newmar Recalls 2018-2019 Motorhomes Due to Loose Brake Caliper Bolts

    Newmar is recalling 2018-2019 Essex, Ventana, and London Aire motorhomes because brake caliper mounting bolts may be loose, increasing crash risk.

    Product
    NEWMAR — NEWMAR VENTANA LE, VENTANA, ESSEX, LONDON AIRE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·085-2018 EXP·2018-12-04

    JBS Tolleson Recalls Raw Beef Products Due to Salmonella Newport

    JBS Tolleson is recalling approximately 12.1 million pounds of raw beef products, including ground beef, due to possible Salmonella Newport contamination.

    Product
    JBS Tolleson Inc. — JBS Tolleson, Inc. Recalls Raw Beef Products due to Possible Salmonella Newport Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • HighCPSC·19720·2018-12-04

    Foremost Recalls Glass Shower Doors and Panels Due to Hinge Failure

    Foremost is recalling about 700 glass shower doors and panels because pivot hinges can fail, causing the glass to separate from the frame and fall or shatter.

    Product
    Glass shower doors and panels
    Category
    Consumer Product
    Distribution
    Distributed nationwide