The Recall Desk

State

US Virgin Islands product recalls

73,738 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 73,738 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

37651–37675 of 73916

  • HighFDA (Food)·F-1900-2018·2018-08-08

    Griffith Labs Recalls Seasoned Crouton Seasoning Due to Salmonella Risk

    Griffith Labs U.S.A. is recalling 183 bags of Seasoned Crouton Seasoning N5 due to the potential presence of Salmonella from a recalled whey ingredient.

    Product
    Seasoned Crouton Seasoning N5 50 pound bag Item 1000011143
    Category
    Food
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-1774-2018·2018-08-08

    Mondelez Recalls Ritz Bits Cheese Big Bags Due to Salmonella Risk

    Mondelez Global is recalling Ritz Bits Cheese Big Bags because a supplier's whey powder ingredient may contain Salmonella.

    Product
    RITZ BITS CHEESE BIG BAG 3 Oz, Pouch Retail: 12 per case Foodservice: 36 per case
    Category
    Food
    Distribution
    2 states
  • HighFDA (Food)·F-1899-2018·2018-08-08

    Griffith Labs Recalls Romano Garlic Seasoning Due to Salmonella Risk

    Griffith Labs U.S.A. is recalling 50-pound bags of Romano Garlic Seasoning due to potential Salmonella contamination from a recalled whey ingredient.

    Product
    Romano Garlic Seasoning 50 pound bag Item 1000015205
    Category
    Food
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1024-2018·2018-08-08

    West-Ward Recalls Doxycycline Hyclate Tablets for Dissolution Failures

    West-Ward Columbus Inc is recalling Doxycycline Hyclate 100 mg tablets because they failed to meet dissolution specifications.

    Product
    DOXYCYCLINE HYCLATE — DOXYCYCLINE HYCLATE (DOXYCYCLINE HYCLATE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2569-2018·2018-08-08

    Stryker FlowGate2 Balloon Guide Catheter Recalled for Diameter Defect

    Stryker Neurovascular is recalling FlowGate2 Balloon Guide Catheters because the balloon diameter may exceed specifications, potentially causing resistance during use.

    Product
    FlowGate2 Balloon Guide Catheter, UPN 90485 (8Fx85cm size) and 90495 (8Fx95cm size)
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2581-2018·2018-08-08

    GE Healthcare Recalls CT Systems with Potential Electrical Wiring Defect

    GE Healthcare is recalling 42 Discovery RT CT systems nationwide due to a potential wiring defect in the electrical panel that may affect the uninterruptible power supply.

    Product
    Discovery RT labeled as: a. MID BJG; b. HVY BJG
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-2588-2018·2018-08-08

    bioMerieux Recalls VIDAS LH Test Kits Due to Calibration Issues

    bioMerieux, Inc. is recalling VIDAS LH test kits because internal tests confirmed a decrease in strip signal over time, leading to invalid calibration results.

    Product
    VIDAS LH, Reference Numbers 30406 and 30406-01. Poduct Usage: VIDAS LH is an automated quantitative test for use on the VIDAS family instruments for the determination of human luteinizing hormone in human serum or plasma (lithium heparin), using the ELFA technique (Enzyme…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-1033-2018·2018-08-08

    Renaissance Lakewood Recalls Fluconazole Injection Bags for Out-of-Specification Levels

    Renaissance Lakewood, LLC is recalling 12,088 bags of Fluconazole Injection because the lots are out of specification for elevated sodium chloride and fluconazole assay levels.

    Product
    Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 200 mg in 100 mL (2 mg/mL), 100 mL Single Dose Flexible Container bag, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902; By: Claris Injectables Ltd., Gujarat, India, NDC a)…
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1031-2018·2018-08-08

    Renaissance Lakewood Recalls Fluconazole Injection Bags Due to Stability Failures

    Renaissance Lakewood, LLC is recalling 3,000 bags of Fluconazole Injection due to elevated sodium chloride and water vapor levels.

    Product
    Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 400 mg in 200 mL (2 mg/mL), 200 mL Single Dose Flexible Container bag, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902; By: Claris Injectables Ltd., Gujarat, India; NDC 36000-003-06.
    Category
    Drug
    Distribution
    Distributed nationwide
  • LowFDA (Drugs)·D-1032-2018·2018-08-08

    Fluconazole Injection Recalled for Elevated Water Vapor Levels

    Renaissance Lakewood, LLC is recalling Fluconazole Injection bags due to elevated water vapor levels. The recall covers 3,664 bags distributed nationwide and in Puerto Rico.

    Product
    Fluconazole Injection, USP, Iso-Osmotic Sodium Chloride Diluent, 200 mg in 100 mL (2 mg/mL), 100 mL Single Dose Flexible Container bag, Rx only, Manufactured for: Claris Lifesciences Inc., North Brunswick, NJ 08902; By: Claris Injectables Ltd., Gujarat, India, NDC 36000-002-10.
    Category
    Drug
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V520000·2018-08-07

    Terex Recalls 2015-2018 Digger Derricks Due to Weld Defect

    Terex is recalling 2015-2018 C4000, C5000, C6000, and General 80 digger derricks because undersized welds may cause the auger to fall unexpectedly, posing an injury risk.

    Product
    TEREX — TEREX C4000, GENERAL 80, C6000, C5000
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V521000·2018-08-07

    BYD Recalls 2016-2017 K11 M Buses Due to Brake Caliper Defect

    BYD is recalling 2016-2017 K11 M hybrid buses because a brake caliper guide pin may break, potentially causing loss of braking ability or tire pressure.

    Product
    BYD — BYD K11 M
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V517000·2018-08-06

    Micro Bird Transit Bus Recall for Seat Belt Anchorage Defect

    Micro Bird is recalling 2015-2018 G5, MB II, and T-Series transit buses because seat belt anchorage plates may not be correctly attached, increasing injury risk in crashes.

    Product
    MICRO BIRD — MICRO BIRD G5 TRANSIT BUS, T-SERIES TRANSIT BUS, MB II TRANSIT BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V519000·2018-08-06

    Garden State Recalls 2015 Double Deck Buses for Emergency Exit Defect

    Garden State Bus Group is recalling 2015 Double Deck Buses because the roof emergency exit is incorrectly located, potentially delaying evacuation during an emergency.

    Product
    GARDEN STATE — GARDEN STATE DOUBLE DECK BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18E079000·2018-08-06

    Hale Recalls Kubota Diesel Pumps Due to Wiring Defect

    Hale Products Inc is recalling Kubota Diesel Powered Portable Pumps because improper wiring may prevent warning lamps from illuminating, increasing the risk of injury if the engine fails.

    Product
    EQUIPMENT recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V516000·2018-08-06

    Micro Bird Recalls 2015-2018 School Buses for Seat Belt Defect

    Micro Bird is recalling 2015-2018 G5, MB II, and T-Series school buses because seat belt anchorage plates may not be correctly attached, increasing injury risk in a crash.

    Product
    MICRO BIRD — MICRO BIRD G5 SCHOOL BUS, MB II SCHOOL BUS, T-SERIES SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·18V518000·2018-08-06

    Newmar Recalls 2018-2019 Motorhomes Due to Door Latch Adjustment Issue

    Newmar is recalling 2018-2019 motorhomes because improperly adjusted door latch rods may allow the entry door to open during transit.

    Product
    NEWMAR — NEWMAR DUTCH STAR, VENTANA LE, VENTANA, ESSEX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·066-2018·2018-08-03

    Star Natural Meats Recalls Raw Pork Sausage for Undeclared Allergens

    Star Natural Meats is recalling raw pork sausage products because they contain undeclared milk, soy, and restricted ingredients.

    Product
    Star Natural Meats LLC — Star Natural Meats, LLC Recalls Raw Pork Sausage Products due to Misbranding and Undeclared Allergens
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·18V513000·2018-08-03

    Mercedes-Benz Recalls 2018 E 400 Cabrio for Child Seat Anchor Defect

    Mercedes-Benz is recalling 2018 E 400 Cabrio vehicles because the child seat anchoring system may not be properly installed, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ E 400
    Category
    Vehicle
    Distribution
    Distributed nationwide