The Recall Desk

State

US Virgin Islands product recalls

73,806 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 73,806 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

44276–44300 of 73984

  • ModerateFDA (Devices)·Z-1431-2017·2017-03-15

    Merge PACS Software Recalled for Telmed Protocol Data Propagation Failures

    Merge Healthcare is recalling specific versions of Merge PACS software because studies may fail to propagate or import via the telmed protocol.

    Product
    Merge PACS software. The firm name on the label is Merge Healthcare.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1422-2017·2017-03-15

    Siemens Biograph 6 TruePoint PET/CT Recall for Missing Instructions

    Siemens is recalling 18 Biograph 6 TruePoint mobile PET/CT systems because mobile-specific instructions were not shipped to a limited population.

    Product
    Biograph 6 TruePoint, Material Number 10097289 The Biograph Mobile PET/CTs are intended to be utilized by appropriately trained health care professionals to: ¿ Image and measure the distribution of injected positron emitting radiopharmaceuticals in humans for the purpose of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1425-2017·2017-03-15

    Siemens Biograph Mobile PET/CT Recall for Missing Instructions

    Siemens is recalling four Biograph Mobile PET/CT units because specific mobile instructions were not shipped to a limited population.

    Product
    Biograph 16 TruePoint TrueV - 4R, Material Number 10249556 The Biograph Mobile PET/CTs are intended to be utilized by appropriately trained health care professionals to: ¿ Image and measure the distribution of injected positron emitting radiopharmaceuticals in humans for the…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0515-2017·2017-03-15

    Sandoz Recalls Pioglitazone and Glimepiride Tablets Due to Dissolution Failure

    Sandoz Inc is recalling specific lots of Pioglitazone and Glimepiride Tablets because they failed to meet dissolution specifications.

    Product
    Pioglitazone and Glimepiride Tablets, USP, 30 mg/4 mg, 30 count bottles, Rx only, Manufactured by Lek Pharmaceuticals d.d., Verovskova Ulica 57, Ljubljana, - SI-1526, Slovenia --- NDC 0781-5635-31
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1419-2017·2017-03-15

    Siemens Progesterone Test Recalled Due to DHEA-S Interference

    Siemens Healthcare Diagnostics is recalling Dimension Vista LOCI Progesterone tests because DHEA-S causes falsely elevated results.

    Product
    Dimension Vista LOCI Progesterone; Catalog Number: K6464; Siemens Material Number: 10461743 Product Usage: For in vitro diagnostic use in the quantitative determination of progesterone in serum and using the ADVIA Centaur¿, ADVIA Centaur XP, ADVIA Centaur XPT and ADVIA…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1418-2017·2017-03-15

    Siemens ADVIA Centaur Progesterone Test Recalled for DHEA-S Interference

    Siemens Healthcare Diagnostics is recalling ADVIA Centaur Progesterone tests because DHEA-S causes falsely elevated results.

    Product
    ADVIA Centaur Progesterone; Catalog Number: 10310305 10315522 10333111 Product Usage: The PROG method is an in vitro diagnostic test for the quantitative measurement of progesterone in human serum and plasma on the Dimension Vista¿System. Progesterone measurements are used…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1423-2017·2017-03-15

    Siemens Biograph Mobile PET/CT Recall for Missing Instructions

    Siemens Medical Solutions is recalling six Biograph Mobile PET/CT units because mobile-specific instructions were not shipped to a limited population of systems.

    Product
    Biograph 6 TruePoint, Material Number 10097290 The Biograph Mobile PET/CTs are intended to be utilized by appropriately trained health care professionals to: ¿ Image and measure the distribution of injected positron emitting radiopharmaceuticals in humans for the purpose of…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • LowFDA (Devices)·Z-1410-2017·2017-03-15

    Integra UNI-CP System Recalled for Incorrect Labeling

    Integra LifeSciences Corp. is recalling 39 units of the UNI-CP System due to incorrect labeling on the plate.

    Product
    The UNI-CP System; Model Number: 330230SND.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V174000·2017-03-14

    Navistar Recalls International Trucks Due to Air Dryer Bracket Fracture Risk

    Navistar is recalling 2016-2018 International heavy diesel trucks because a mounting bracket may fracture, causing air leaks and increased stopping distance.

    Product
    INTERNATIONAL — INTERNATIONAL PROSTAR, LONESTAR, LT, RH
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V178000·2017-03-14

    Mercedes-Benz Recalls 2016 G550 and G63 Due to Door Cable Defect

    Mercedes-Benz is recalling 2016 G550 and G63 vehicles because a door cable may break, preventing occupants from opening the door from inside after a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ G550, G63
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V175000·2017-03-14

    Altec Recalls 2015-2016 Aerial Devices and Service Body Trucks

    Altec is recalling 2015-2016 Aerial Devices and Service Body Trucks due to a wiring defect that may cause a short circuit and increase fire risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE, SERVICE BODY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V173000·2017-03-14

    Volvo Bus Recalls 2016-2017 9700 Models for Engine Stall Risk

    Volvo Bus is recalling 2016-2017 9700 transit buses because a ground cable may be improperly installed, causing the engine to stall unexpectedly.

    Product
    VOLVO BUS — VOLVO BUS 9700
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V167000·2017-03-14

    Jayco Recalls 2017 Designer Fifth Wheels Due to Spare Tire Rubbing

    Jayco is recalling 2017 Designer fifth wheel trailers because the spare tire rim may rub against the brake caliper, increasing crash risk.

    Product
    JAYCO FIFTH WHEEL — JAYCO FIFTH WHEEL DESIGNER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·17109·2017-03-14

    Energizer XBOX ONE 2X Smart Chargers Recalled Due to Burn Hazard

    Performance Designed Products is recalling Energizer XBOX ONE 2X Smart Chargers because they can overheat and damage controllers, posing a burn risk.

    Product
    Energizer® XBOX ONE 2X Smart Chargers
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·17V171000·2017-03-14

    Forest River Cherokee Recalled for Incorrect Federal Tire Placard Information

    Forest River is recalling 2017 Cherokee recreational trailers because the Federal Placard lists incorrect tire and rim sizes, which may lead to installing wrong replacement tires.

    Product
    FOREST RIVER — FOREST RIVER CHEROKEE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V177000·2017-03-14

    Mercedes-Benz Recalls Vehicles Due to Potential Air Bag Deployment Issues

    Mercedes-Benz is recalling various models because incorrect software in control units may prevent air bags from deploying correctly in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ, MERCEDES BENZ C250, C300, C350, CLS550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·17V176000·2017-03-14

    Mercedes-Benz Recalls 2017 E300 Models for Front Passenger Air Bag Defect

    Mercedes-Benz is recalling 2017 E300 and E300 4Matic vehicles because the front passenger air bag may not deploy properly in certain seating positions, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E300
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V160000·2017-03-13

    Spartan Trucks Recalled for Front Suspension Ball Joint Separation Risk

    Spartan Motors is recalling specific 2011-2018 trucks because front suspension ball joints can loosen, potentially causing a loss of steering control.

    Product
    SPARTAN — SPARTAN GLADIATOR, K4, METROSTAR, K3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V168000·2017-03-13

    Ford Recalls 2017 Mustangs for Door Handle Spring Defect

    Ford is recalling 2017 Mustangs because the driver-side door handle spring may loosen, allowing the door to unlatch in a crash.

    Product
    FORD — FORD MUSTANG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V170000·2017-03-13

    Roush-Modified Ford Propane Vehicles Recalled for Fuel Valve Defect

    Roush CleanTech is recalling 2015-2017 modified Ford E-450, F59, F-650, and F-750 vehicles because a fuel control valve solenoid may short circuit, causing the engine to shut off while driving.

    Product
    FORD — FORD F59 ROUSH PROPANE, F-650 ROUSH PROPANE, F-750 ROUSH PROPANE, E-450 ROUSH PROPANE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17E017000·2017-03-13

    Roush Propane Conversion Kit Recall for Fuel Valve Short Circuit

    Roush CleanTech is recalling Generation 4 Propane Conversion Kits because a fuel control valve solenoid may short circuit, causing the engine to shut off while driving.

    Product
    FUEL SYSTEM, OTHER recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·17V161000·2017-03-13

    Maserati Recalls 2017 Levante Models Due to Engine Software Defect

    Maserati is recalling 2017 Levante vehicles because an engine software issue may cause the transmission to shift into neutral or the engine to shut off at slow speeds.

    Product
    MASERATI — MASERATI LEVANTE
    Category
    Vehicle
    Distribution
    Distributed nationwide