The Recall Desk

State

US Virgin Islands product recalls

73,827 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.

Which agencies issued them

These figures cover only the 178 recalls whose distribution notice names US Virgin Islands specifically. The 73,827 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

56276–56300 of 74005

  • LowFDA (Devices)·Z-0234-2015·2014-11-26

    Biomerieux Recalls Etest Ceftaroline Devices Due to Incorrect Expiration Date

    Biomerieux is recalling 652 Etest Ceftaroline devices because the labeling displays a 5-year expiration instead of the correct 2-year period.

    Product
    Etest¿ Ceftaroline (CPT32) US B30. Etest¿ (Antimicrobial Susceptibility Testing) is a quantitative technique for determining the antimicrobial susceptibility of Gram negative and Gram positive aerobic bacteria.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereCPSC·15036·2014-11-25

    Goal Zero Sherpa 50 and 120 Battery Packs Recalled for Fire Hazard

    Goal Zero is recalling Sherpa 50 and 120 rechargeable battery packs because they can overheat and catch fire. Consumers should stop using the units and contact the company for a free replacement.

    Product
    Goal Zero Sherpa brand 50 and 120 rechargeable battery packs
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·14V753000·2014-11-25

    Aston Martin Recalls 2006-2014 Models for Seat Heater Overheating Risk

    Aston Martin is recalling 7,256 vehicles because a faulty seat heater module may prevent the heaters from turning off, creating a risk of overheating and injury.

    Product
    ASTON MARTIN — ASTON MARTIN V8 VANTAGE, DBS, DB9, V12 VANTAGE COUPE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15037·2014-11-25

    Pro Armor Recalls Utility Vehicle Doors Due to Latch Failure

    Pro Armor is recalling about 300 utility vehicle doors for Polaris RZR models because the latch pin can disengage, posing impact and laceration hazards.

    Product
    Utility vehicle doors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V751000·2014-11-24

    Capacity Recalls 2014 ISB13 Trucks Due to Fuel Filter Defect

    Capacity is recalling 2014 ISB13 trucks because a fuel filter defect may cause the engine to stall without warning, increasing the risk of a crash.

    Product
    CAPACITY — CAPACITY ISB13
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V750000·2014-11-24

    Harley-Davidson Recalls 2015 Tri-Glide Motorcycles Due to Rear Brake Defect

    Harley-Davidson is recalling 1,560 model year 2015 Tri-Glide motorcycles because a defective rear brake master cylinder piston may cause brake failure and increase crash risk.

    Product
    HARLEY-DAVIDSON — HARLEY-DAVIDSON FLHTCUTG
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V747000·2014-11-24

    Spartan Trucks Recalled for Air Brake Valve Defect

    Spartan is recalling 2013-2015 trucks because damaged air brake valves may reduce braking performance or cause parking brakes to reapply, increasing crash risk.

    Product
    SPARTAN — SPARTAN GLADIATOR, DR, NVS, MM
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V748000·2014-11-24

    Champion Transit Bus Recall for Defective Passenger Seat Spring Nuts

    Champion is recalling 2014-2015 transit buses because defective spring nuts may fail to secure passenger seats, increasing injury risk in a crash.

    Product
    CHAMPION — CHAMPION CHALLENGER, CRUSADER, DEFENDER, HCAC
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereUSDA FSIS·082-2014·2014-11-22

    Ranchers Legacy Recalls Ground Beef Products Due To E. Coli O157:H7 Risk

    Ranchers Legacy Meat Co. is recalling 1,200 pounds of ground beef products produced on Nov. 19, 2014, due to possible E. coli O157:H7 contamination.

    Product
    Rancher's US OP LLC — Minnesota Firm Recalls Ground Beef Products Due To Possible E. Coli O157:H7 Contamination
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V746000·2014-11-21

    Terex Recalls 2014 Light Tower AL5 Work Platforms Due to Fuel Tank Defect

    Terex is recalling 84 model year 2014 Light Tower AL5 work platforms because insufficient structural support on the fuel tank could cause it to deform and contact the trailer axle, increasing fire risk.

    Product
    TEREX — TEREX LIGHT TOWER AL5
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·14V745000·2014-11-21

    Altec Recalls Aerial Devices Due to Hydraulic Pressure Transducer Defect

    Altec is recalling 1999-2014 aerial devices because an improperly set hydraulic pressure transducer may cause inadvertent boom movement in cooler temperatures, increasing injury risk.

    Product
    ALTEC — ALTEC AERIAL DEVICE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15032·2014-11-20

    Graco Recalls 11 Stroller Models Due to Fingertip Amputation Hazard

    Graco is recalling 11 stroller models because the folding hinge can pinch a child's finger, causing lacerations or amputations.

    Product
    Aspen, Breeze, Capri, Cirrus, Glider, Kite, LiteRider, Sierra, Solara, Sterling and TravelMate Model Strollers and Travel Systems
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereNHTSA·14V738000·2014-11-20

    Mack Trucks Recalls 2015 Pinnacle and Granite Models for Wiring Defect

    Mack Trucks is recalling 2015 Pinnacle and Granite trucks because an incorrectly wired system may fail to control engine speed, increasing the risk of fire.

    Product
    MACK — MACK PINNACLE (CXU), GRANITE (GU)
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·15709·2014-11-20

    Tyco Recalls Simplex Fire Alarm Panels Due to Activation Failure

    Tyco is recalling about 750 Simplex 4100ES fire alarm control panels because a defective chip can prevent the system from activating during an alarm, posing a risk of injury and property damage.

    Product
    Simplex 4100ES Fire Alarm Control Panel
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15035·2014-11-20

    Leatherman Recalls Children's Multi-Tool Due to Laceration Hazard

    Leatherman is recalling the Leap multi-tool because the optional knife blade can inadvertently release, posing a laceration hazard. No injuries have been reported.

    Product
    Leatherman® Leap™ multi-tool
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighCPSC·15708·2014-11-20

    Bob-Cat Recalls Zero Turn Riding Mowers Due to Crash Hazard

    Bob-Cat is recalling about 4,900 zero turn riding mowers because the steering control arm can break, causing the driver to lose control and crash.

    Product
    Bob-Cat Zero Turn Riding Mower
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • CriticalFDA (Devices)·Z-0171-2015·2014-11-19

    Siemens MicroScan Rapid Urine Combo Panel Recalled for False Positive Results

    Siemens Healthcare Diagnostics is recalling Rapid Neg Urine Combo Panel Type 1 due to an increase in false positive susceptible results when used with MicroScan Microbiology Systems.

    Product
    Rapid Neg Urine Combo Panel Type 1; Catalog number B 1017-167; Siemens Material Number 10444652 MicroScan Rapid panels are designed for use in determining identification to the species level and/or antimicrobial agent susceptibility of rapidly growing aerobic and…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • CriticalFDA (Food)·F-0491-2015·2014-11-19

    Protein Supplement Recalled for Undeclared Milk Allergen

    Maine Natural Health, Inc. is recalling Fortified Vanilla Dietary Supplement because it fails to declare milk as an allergen.

    Product
    Fortified Vanilla Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0475-2015·2014-11-19

    Maine Natural Health Recalls Pure Whey Chocolate for Undeclared Milk

    Maine Natural Health is recalling Pure Whey Chocolate dietary supplements because the labels fail to declare the allergen milk.

    Product
    Pure Whey Chocolate, Dietary Supplement Packaged under the labels: Maine Natural Health and Stronger Faster Healthier Packaged in: 2 lb (32 oz), 10 oz.
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0184-2015·2014-11-19

    GE Healthcare Infinia Nuclear Medicine Systems Recalled for Loose Fasteners

    GE Healthcare is recalling Infinia nuclear medicine systems because loose fasteners could cause a portion of the system to fall onto a patient during a scan.

    Product
    GE Healthcare Infinia (including Infinia, Infinia Hawkeye, Infinia II, Infinia II Hawkeye, Infinia II Hawkeye 4, Infinia II VC, Infinia II VC Hawkeye, and Infinia II VC Hawkeye 4) Models: H3000WC, H3000WD, H3000WE, H3000WM, H3000WN, H3000WP, H3000WR, H3000WT, H3000WW, H3000WY…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0493-2015·2014-11-19

    Maine Natural Health Recalls Rejuvenate Vanilla Protein Supplement for Undeclared Milk

    Maine Natural Health, Inc. is recalling Rejuvenate Vanilla Dietary Supplement because it fails to declare the allergen milk. The product was distributed nationwide in 2 lb and 10 oz sizes.

    Product
    Rejuvenate Vanilla Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0487-2015·2014-11-19

    Daily Balance Chocolate Dietary Supplement Recalled for Undeclared Milk Allergen

    Maine Natural Health, Inc. is recalling Daily Balance Chocolate Dietary Supplement because it fails to declare the milk allergen.

    Product
    Daily Balance Chocolate Dietary Supplement Packaged under the labels Stronger Faster Healthier: 2 lb (32 oz), and 10 oz sizes
    Category
    Food
    Distribution
    Distributed nationwide