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.

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.

55451–55475 of 74005

  • HighNHTSA·15E008000·2015-02-13

    Recaro Bus Driver Seats Recalled for Seat Belt Retraction Defect

    Johnson Controls is recalling Recaro bus driver seats where a tether bar may interfere with the seat belt locking mechanism, increasing injury risk in crashes.

    Product
    SEAT BELTS:FRONT:RETRACTOR recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·15E007000·2015-02-13

    Airtex Fuel Pump Modules Recalled Due to Fuel Leak Fire Risk

    Airtex is recalling specific fuel pump modules because an improper seal may cause fuel leaks, increasing the risk of a fire.

    Product
    FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP recall
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereCPSC·15070·2015-02-12

    Jackco ZETA Pocket Jump Starter Recalled for Fire Hazard

    Jackco Transnational is recalling ZETA Pocket Jump Starters because the battery packs can overheat and catch fire. Consumers should stop using the product and contact the company for a refund.

    Product
    ZETA by Jackco Pocket Jump Starter - Deluxe Set
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1059-2015·2015-02-11

    Siemens LINAC Accelerators Recalled for Overheating and Smoke Emission

    Siemens Medical Solutions is recalling 310 LINAC Accelerators because the internal electric board may overheat, causing thermal damage and smoke emission.

    Product
    LINAC Accelerators: ARTISTE, ONCOR Avant Garde, ONCOR Impression Plus, ONCOR Expression, ONCOR Impression, PRIMUS HI, Mevatron M2/Primus Mid-Energy, MEVATRON PRIMART, MEVATRON KD-2, MEVATRON KDS-2, MEVATRON KDS-2, MEVATRON KD-2, MEVATRON K2, MEVATRON 6323-2, MEVATRON…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V084000·2015-02-11

    Navistar Recalls 2015-2016 IC CE School Buses for Fuel Leak Risk

    Navistar is recalling 6,302 model year 2015-2016 IC CE school buses because the powertrain wiring harness may contact a high-pressure fuel line, potentially causing a fuel leak and fire.

    Product
    IC BUS — IC BUS CASB, CESB
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1054-2015·2015-02-11

    Cardinal Health Recalls Lubricated Intubating Stylets Due to Shear Risk

    Cardinal Health is recalling 104,432 Lubricated Intubating Stylets 6FR because a small piece of the sheath may shear off during removal, posing a risk to infants and pediatric patients.

    Product
    Lubricated Intubating Stylet 6FR that is inserted into an endotracheal tube to facilitate intubation. This product is used in surgical or medical emergency facilities. Primarily used on infants and pediatric patients.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1017-2015·2015-02-11

    FDA Recalls Covidien Trellis-6 Peripheral Infusion Systems Due to Labeling Error

    The FDA is recalling 216 units of the Covidien Trellis-6 Peripheral Infusion System because a manufacturing error caused the balloon inflation ports to be incorrectly labeled.

    Product
    Covidien Trellis-6 Peripheral Infusion System. Models BVT608010V01, BVT608030V01, BVT612010V01, and BVT612030V01. Sterile EO. Product Usage: Intended for controlled and selective infusion of physician-specified fluids, including thrombolytics, into the peripheral…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0958-2015·2015-02-11

    Reily Foods Recalls Chili Kits for Undeclared Peanut and Almond Allergens

    Reily Foods is recalling Wick Fowler's Famous Texas Style 2-Alarm Chili Kits because they contain peanut and almond allergens that are not declared on the ingredient statements.

    Product
    WICK FOWLER'S FAMOUS TEXAS STYLE 2-ALARM Chili Kit, NET WT. 3.6525 oz. (102g), Dist. by Reily Foods Company, New Orleans, LA 70130, 1-800-535-1961, UPC 0-00-71092-00069-8
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0956-2015·2015-02-11

    Reily Foods Recalls Chili Kits With Undeclared Peanut and Almond Allergens

    Reily Foods is recalling Carroll Shelby's Original Texas Brand Chili Kits because they contain peanut and almond allergens not listed on the ingredient label.

    Product
    CARROLL SHELBY'S ORIGINAL TEXAS BRAND CHILI KIT, NET WT. 4 oz. (113 g), Dist. by Reily Foods Company, New Orleans, LA 70130, 1-800-535-1961, UPC 0-00-72396-10000-8
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereNHTSA·15V086000·2015-02-11

    Airstream Recalls 2014-2015 Travel Trailers Due to Propane Tank Screw Failure

    Airstream is recalling 2014-2015 travel trailers because screws securing the propane tank tray may fail, allowing tanks to fall and cause fire or collision.

    Product
    AIRSTREAM — AIRSTREAM FLYING CLOUD, INTERNATIONAL, LAND YACHT, SPORT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-1018-2015·2015-02-11

    FDA Recalls Covidien Trellis-8 Peripheral Infusion Systems Due to Labeling Error

    FDA is recalling 1,032 units of the Covidien Trellis-8 Peripheral Infusion System because a manufacturing error caused the proximal and distal balloon inflation ports to be incorrectly labeled.

    Product
    Covidien Trellis-8 Peripheral Infusion System. Models CVT808015, CVT808025, CVT812015, and CVT812025. The following models are not offered for sale in the US: EVT808015, EVT808025, EVT812015, and EVT812025 Sterile EO. Product Usage: Intended for controlled and selective…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0957-2015·2015-02-11

    Reily Foods Recalls White Chicken Chili Kits Due to Undeclared Allergens

    Reily Foods is recalling Carroll Shelby's Original Texas Brand White Chicken Chili Kits because they contain peanut and almond allergens not listed on the ingredient label.

    Product
    CARROLL SHELBY'S ORIGINAL TEXAS BRAND WHITE CHICKEN CHILI KIT, 3 oz. (85 g), Dist. by Reily Foods Company, New Orleans, LA 70130, UPC 0-00-72396-10019-0
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Food)·F-0959-2015·2015-02-11

    Reily Foods Recalls Wick Fowler's Chili Kits for Undeclared Allergens

    Reily Foods is recalling Wick Fowler's Texas Style False Alarm Mild Chili Kits because they contain peanut and almond allergens that are not declared on the ingredient statements.

    Product
    WICK FOWLER'S TEXAS STYLE FALSE ALARM Mild Chili Kit, NET WT. 3.03 oz. (86g), Dist. by Reily Foods Company, New Orleans, LA 70130, UPC 0-00-71092-00111-4
    Category
    Food
    Distribution
    Distributed nationwide
  • SevereFDA (Drugs)·D-0382-2015·2015-02-11

    Hospira Recalls Lidocaine Hydrochloride Injection Due to Particulate Matter

    Hospira Inc. is recalling 120,900 vials of 1% Lidocaine Hydrochloride Injection because iron oxide particulates were found in the solution.

    Product
    LIDOCAINE HYDROCHLORIDE — LIDOCAINE HYDROCHLORIDE (LIDOCAINE HYDROCHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1036-2015·2015-02-11

    Invacare Recalls G-Series Bed Rails Due to Entrapment Safety Defect

    Invacare is recalling G-Series bed rails because the mounting bracket does not meet entrapment safety specifications.

    Product
    G- Series Beds; G29 full length bed rails assembly
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1042-2015·2015-02-11

    Zimmer Persona Tibial Inserter Recalled for Potential Tip Fracture

    Zimmer, Inc. is recalling 1,091 Persona Tibial Articular Surface Inserters due to a potential fracture of the instrument tip, which could cause tissue damage or require revision surgery.

    Product
    Zimmer PERSONA Tibial Articular Surface Inserter; Item # 42-5299-001-00. Manual surgical instrument for knee arthroplasty (orthopedic).
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·15077·2015-02-11

    System Sensor Recalls Combination Carbon Monoxide and Smoke Detectors

    System Sensor is recalling i4 Series combination CO/smoke detectors because they may fail to detect carbon monoxide, posing a poisoning risk.

    Product
    i4 Series System Sensor combination carbon monoxide (CO)/smoke detectors
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1038-2015·2015-02-11

    SCC Soft Computer Recalls SoftLab Laboratory Information System Versions

    SCC Soft Computer is recalling SoftLab versions 4.0.7.0 and 4.0.7.1 because the software fails to send abnormal flags for Reference Lab test results.

    Product
    SoftLab with SA HIS versions 4.0.7.0-4.0.7.1 SoftLab is a laboratory information system to be used in a medical research or clinical laboratory.
    Category
    Medical Device
    Distribution
    Distributed nationwide