The Recall Desk

State

US Virgin Islands product recalls

73,597 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 73,597 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

29501–29525 of 73775

  • ModerateFDA (Drugs)·D-1042-2020·2020-03-25

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Therapeutics is recalling Daytrana (methylphenidate) patches because the delivery system failed mechanical peel and shear specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1493-2020·2020-03-25

    Philips Allura CV20 X-ray System Recalled for Capacitor Failure

    Philips is recalling 128 Allura CV20 X-ray systems because a capacitor may fail after electrical surges, preventing image acquisition.

    Product
    Allura CV20, system code 722031
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1050-2020·2020-03-25

    Breckenridge Recalls Solifenacin Succinate Tablets Due to Manufacturing Deviations

    Breckenridge Pharmaceutical is recalling specific lots of Solifenacin Succinate Tablets because manufacturing deviations may have resulted in the product converting to Solifenacin Tartrate.

    Product
    Solifenacin Succinate Tablets, 5mg, packaged in a) 30-count bottles (NDC 51991-893-33) and b) 90-count bottles (NDC 51991-893-90) Distributed by: Breckenridge Pharmaceutical, Inc. Boca Raton, FL 33487; Manufactured by: Piramal Enterprises Limited Plot No 67-70, Sector -2…
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1058-2020·2020-03-25

    Jubilant Cadista Recalls Pantoprazole Sodium Tablets Due to CGMP Deviations

    Jubilant Cadista Pharmaceuticals is recalling 89,376 bottles of Pantoprazole Sodium Delayed-Release Tablets due to dark brown discoloration on tablet edges.

    Product
    Pantoprazole Sodium Delayed-Release Tablets, USP, 40 mg, 90 count bottle, Rx Only, Manufactured by Jubilant Generics Ltd, Roorkee-247661 India, NDC 59746-284-90
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1487-2020·2020-03-25

    Philips Integris Allura X-ray Systems Recalled for Capacitor Failure

    Philips is recalling 70 Integris Allura 15 & 12 X-ray systems because a capacitor may fail, preventing image acquisition.

    Product
    Integris Allura 15 & 12, monoplane (system code 722043) and biplane (system code 722044)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1032-2020·2020-03-25

    Sun Pharmaceutical Recalls Doxycycline Capsules Due to Manufacturing Deviations

    Sun Pharmaceutical Industries is recalling 624 bottles of Doxycycline Capsules, 75 mg, because they were not manufactured under Current Good Manufacturing Practice conditions.

    Product
    DOXYCYCLINE — DOXYCYCLINE (DOXYCYCLINE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1045-2020·2020-03-25

    Noven Recalls Daytrana Patches Due to Defective Delivery System

    Noven Therapeutics is recalling Daytrana (methylphenidate) transdermal patches because the delivery system failed mechanical peel and shear specifications.

    Product
    DAYTRANA — DAYTRANA (METHYLPHENIDATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1029-2020·2020-03-25

    Strides Pharma Recalls Potassium Chloride Tablets Due to Oversized Size

    Strides Pharma Science Limited is recalling specific lots of Potassium Chloride Extended-Release Tablets because oversized tablets were found.

    Product
    POTASSIUM CHLORIDE — POTASSIUM CHLORIDE (POTASSIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V175000·2020-03-23

    2021 Ford E-350 and E-450 wire harness may damage fuel pump and ABS

    Ford is recalling 2021 E-350 and E-450 vehicles because a rear wire harness may contact the frame and damage circuits for the fuel pump and anti-lock braking system, potentially causing engine stall or loss of braking control.

    Product
    FORD — FORD E-450, E-350
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V176000·2020-03-23

    Freightliner Trucks Recalled for Axle Lubrication Defect

    Daimler Trucks is recalling 2019-2020 Freightliner M2 and 108SD trucks because insufficient axle lubrication may damage wheel bearings, increasing crash risk.

    Product
    FREIGHTLINER — FREIGHTLINER BUSINESS CLASS M2, 108SD
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V177000·2020-03-23

    Ford Recalls 2014-2016 Vehicles for Door Latch Defect

    Ford is recalling 2014-2016 Fiesta, Fusion, and Lincoln MKZ vehicles because a door latch component may break, causing doors to open while driving.

    Product
    LINCOLN — LINCOLN, FORD MKZ, FUSION, FIESTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V168000·2020-03-20

    Terex Recalls 2009-2016 Aerial Devices Due to Lift Cylinder Defect

    Terex is recalling 2009-2016 TCX and SML aerial devices because lift cylinder rod eyes may fail, causing the boom to drift down and increasing injury risk.

    Product
    TEREX — TEREX SML, TCX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V171000·2020-03-20

    Newmar Recalls Motorhomes Due to Insufficiently Tightened Brake Caliper Bolts

    Newmar is recalling specific 2019-2020 motorhomes because brake caliper mounting bolts may be loose, which can reduce braking effectiveness and increase crash risk.

    Product
    NEWMAR — NEWMAR LONDON AIRE, ESSEX, VENTANA, VENTANA LE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20V173000·2020-03-20

    Mercedes-Benz Recalls S560 Vehicles Due to Engine Oil Plug Defect

    Mercedes-Benz is recalling 2018-2019 S560 and Maybach S560 vehicles because engine oil plugs may fail under high load, causing oil leaks or engine stalls that increase crash risk.

    Product
    MERCEDES-MAYBACH — MERCEDES-MAYBACH, MERCEDES-BENZ S 560 4MATIC, S560
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E016000·2020-03-20

    Harbor Freight Recalls Pittsburgh Automotive 6 Ton Heavy Duty Steel Jack Stands

    Harbor Freight is recalling 454,000 Pittsburgh Automotive 6 Ton Heavy Duty Steel Jack Stands because the ratchet teeth may not engage properly, risking sudden failure and injury.

    Product
    EQUIPMENT:MECHANICAL:INTEGRATED JACK/LEVELER/STABILIZER recall
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·20E015000·2020-03-20

    Carrier Trailer Refrigeration Units Recalled for Fire Risk

    Carrier is recalling 107 trailer refrigeration units because a generator harness may chafe, causing electrical arcing and increasing the risk of a fire.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·20E014000·2020-03-20

    Carrier Truck Refrigeration Units Recalled for Fire Risk

    Carrier is recalling certain Transicold Supra series truck refrigeration units because improperly routed cables may chafe and cause a fire.

    Product
    EQUIPMENT:ELECTRICAL recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·20V158000·2020-03-19

    Forest River Recalls Vans Due to Transmission Shifter Cable Separation

    Forest River is recalling 2016-2020 vans because the transmission shifter cable may disconnect, causing unintended vehicle movement and crash risk.

    Product
    LONE STAR HANDICAP VANS — LONE STAR HANDICAP VANS, FOREST RIVER, COACHMEN L1 VAN, REV, ORION
    Category
    Vehicle
    Distribution
    Distributed nationwide