The Recall Desk

State

US Virgin Islands product recalls

73,509 recalls have nationwide distribution and so reach US Virgin Islands. 177 additional recalls listed US Virgin Islands specifically in their distribution scope.

What the numbers show

Total
177
Critical
12
Severe
39
Most recent
2026-10-14

Of the 177 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 177 recalls whose distribution notice names US Virgin Islands specifically. The 73,509 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25776–25800 of 73686

  • HighNHTSA·21V110000·2021-02-24

    2021-2022 Polestar 2 vehicles recalled for battery control software glitch

    Polestar is recalling certain 2021-2022 Polestar 2 vehicles. A software issue in the Battery Energy Control Module may cause the high voltage system to disconnect, resulting in loss of drive power and increased crash risk.

    Product
    POLESTAR — POLESTAR POLESTAR 2
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighCPSC·21086·2021-02-24

    Northern Tool Recalls Powerhorse Generators Due to Electrical Shock Hazard

    Northern Tool & Equipment is recalling Powerhorse 13000ES portable generators due to a wiring error that can cause electrical shock. No injuries have been reported.

    Product
    Northern Tool & Equipment Powerhorse 13000ES Portable Generators
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1129-2021·2021-02-24

    GE Healthcare Recalls Revolution CT Systems Due to Table Pinch Protector Issue

    GE Healthcare is recalling 96 Revolution CT systems because a damaged or missing table pinch protector may expose sharp screws, posing a laceration risk.

    Product
    System, X-Ray, Tomography, Computed: Revolution Apex, Revolution CT with Apex Edition
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1130-2021·2021-02-24

    GE Healthcare Recalls Revolution CT Systems Due to Table Pinch Protector Defect

    GE Healthcare is recalling Revolution CT and Revolution CT ES systems because damaged or missing table pinch protectors may expose sharp screws, posing a laceration risk.

    Product
    System, X-Ray, Tomography, Computed: Revolution CT, Revolution CT ES.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighCPSC·21085·2021-02-24

    Potter Electric Recalls Addressable Pull Stations Due to Fire Alarm Failure

    Potter Electric is recalling specific addressable pull stations because the handle may fail to activate the fire alarm, posing a risk of failure to alert occupants to a fire.

    Product
    Potter Electric Addressable Pull Stations Single/Dual Action
    Category
    Consumer Product
    Distribution
    Distributed nationwide
  • HighNHTSA·21V108000·2021-02-24

    Freightliner Custom XC Chassis Recalled for Missing Brake Return Spring

    Daimler Trucks North America is recalling 2021-2022 Freightliner Custom XC Chassis vehicles because a missing brake pedal return spring may cause brake lights to stay on or brakes to remain engaged.

    Product
    FCCC — FCCC XC CHASSIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V111000·2021-02-24

    Audi A8 and S8 Engine Control Module Connector Defect May Cause Engine Stall

    Audi is recalling certain 2019-2021 A8 and 2020-2021 S8 vehicles due to a missing sealing pin on the engine control module connector. Moisture can enter the connector and cause the engine to stall, increasing crash risk.

    Product
    AUDI — AUDI S8, A8
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1116-2021·2021-02-24

    Medtronic Recalls Cerebrospinal Fluid Valves Due to Radiopaque Marking Issues

    Medtronic Neurosurgery is recalling 22,528 units of STRATA II cerebrospinal fluid valves and shunts worldwide because radiopaque markings may vary in visibility under imaging.

    Product
    Medtronic Cerebro Spinal Fluid Flow Control Valves and Shunts. STRATA II Valves and Shunts for the following CFNs: 27739 - SHUNT 27739 STRATA NSC SNAP SML 120CM, 27740 - SHUNT 27740 STRATA NSC SNAP REG 120CM, 27812 - VALVE 27812 STRATA II SM EXTRACTED, 27814 - SHUNT…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1125-2021·2021-02-24

    Confirm Biosciences Recalls Healgen COVID-19 Rapid Test Cassettes

    Confirm Biosciences is recalling Healgen COVID-19 Rapid Test Cassettes because they were distributed to non-certified labs and not validated for fingerstick use.

    Product
    Healgen COVID-19 IgG/IgM Rapid Test Cassette (Whole Blood/Serum/Plasma) REF GCC)V-402a - Product Usage: is a lateral flow immunoassay intended for the qualitative detection and differentiation of IgM and IgG antibodies to SARS-CoV- 2 in human venous whole blood, plasma from…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1128-2021·2021-02-24

    Cairn Diagnostics Recalls 13C-Spirulina Gastric Emptying Breath Test Kits

    Cairn Diagnostics is recalling 103 kits of the 13C-Spirulina Gastric Emptying Breath Test due to a potential for false negative diagnoses of gastroparesis.

    Product
    13C-Spirulina Gastric Emptying Breath Test (GEBT) - Product Usage: intended for use in the measurement of the rate of gastric emptying of solids and as an aid in the diagnosis of delayed gastric emptying (gastroparesis) in adult humans who are symptomatic for gastroparesis.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0257-2021·2021-02-24

    DLC Laboratories Recalls Sulfur Ointment Jars Due to Labeling Error

    DLC Laboratories is recalling 86,297 jars of Sulfur Ointment 10% because English labels for Camphor were incorrectly applied to the product.

    Product
    Sulfur Ointment 10%, Pomada de Azufre, 2.6 OZ (73.7g) jar; Manufactured by/ Fabricado por: De La Cruz Products, A Division of DLC Laboratories, Inc. Paramount, CA 9023 USA; UPC 024286150426
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0264-2021·2021-02-24

    Ascend Recalls Cephalexin Oral Suspension Due to CGMP Deviations

    Ascend Laboratories LLC is recalling Cephalexin for Oral Suspension due to CGMP deviations involving unidentified impurities.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0260-2021·2021-02-24

    Auryxia Tablets Recalled for Failed Dissolution Specifications

    Akebia Therapeutics is recalling Auryxia (ferric citrate) tablets because they failed to meet dissolution specifications.

    Product
    Auryxia (ferric citrate) tablets, 210 mg*, 200 tablets bottle, RX ONLY, Manufactured for and distributed by: KERYX BIOPHARMACEUTICALS, INC., 245 First Street, Suite 1400, Cambridge, MA 02142, USA, NDC 59922-0631-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0263-2021·2021-02-24

    Ascend Recalls Cephalexin Oral Suspension Due to Impurity Levels

    Ascend Laboratories is recalling Cephalexin for Oral Suspension because unidentified impurities were found at higher levels than allowed.

    Product
    CEPHALEXIN — CEPHALEXIN (CEPHALEXIN)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1115-2021·2021-02-24

    Medtronic Delta CSF Valves Recalled for Radiopaque Marking Visibility Issues

    Medtronic is recalling Delta CSF flow control valves because radiopaque markings may not be clearly visible under X-ray imaging.

    Product
    Medtronic Delta CSF (Cerebro Spinal Fluid) -Flow Control Valves for the following CFNs/REF numbers: 24048 - VALVE 24048 DELTA RGL PL 0.5, 24053 - CHAMBER 24053 DELTA, 24147 - VALVE 24147 DELTA SML PL0.5, 25121-1 - ASSY 25121-1 DELTA SML SNAP PERIT 120, 25121-5 - ASSY…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1117-2021·2021-02-24

    Medtronic CSF-Flow Control Valves Recalled for Radiopaque Marking Visibility Issues

    Medtronic Neurosurgery is recalling 20,817 CSF-Flow Control Valves worldwide due to potential variation in radiopaque marking visibility under radiographic imaging.

    Product
    Medtronic PS Medical Cerebro Spinal Fluid (CSF)-Flow Control Valves for the following CFNs: 22011 L- SHUNT 22011 L INTL ONLY ULTRA SM LOW 22011 LL - SHUNT 22011 LL INTL ONLY ULTRA SM L-L 22011 M - SHUNT 22011 M INTL ONLY ULTRA SM MED 22017 B-L - SHUNT 22017 B-L ASSY US…
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1127-2021·2021-02-24

    Sky Medical SARS-CoV-2 Rapid Test Kits Recalled for Lack of Emergency Use Authorization

    Sky Medical Supplies and Equipments LLC is recalling 10,000 SARS-CoV-2 rapid test kits distributed in Florida and Peru because they were sold without FDA Emergency Use Authorization.

    Product
    AntIbody to SARS-CoV-2 - Product Usage: (Colloidal Gold) for IgG/IgM Diagnostic Kit, RAPID TEST DEVICE, Whole Blood/Serum/Plasma, SKY Medical Supplies and Equipments, LLC.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V104000·2021-02-23

    Bentley Recalls One 2020 Flying Spur for Fuel Tank Welding Defect

    Bentley is recalling one 2020 Flying Spur because the fuel tank may not have been welded properly, creating a risk of fuel leak and fire.

    Product
    BENTLEY — BENTLEY FLYING SPUR
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereNHTSA·21V106000·2021-02-23

    Mercedes-Benz Metris Recall for Improperly Welded Front Passenger Seat Frame

    Daimler Vans USA is recalling 2021 Mercedes-Benz Metris vans because the front passenger seat frame base may not have been welded properly, increasing injury risk in a crash.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ METRIS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V101000·2021-02-22

    2021 Mazda Mazda3 and CX-30 tire air valve failure recall

    Mazda is recalling 2021 Mazda3 and CX-30 vehicles because air may leak from the tire air valve, potentially causing loss of vehicle control. Mazda will replace all tire air valves at no cost.

    Product
    MAZDA — MAZDA CX-30, MAZDA3
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·21V102000·2021-02-22

    Mercedes-Benz Recalls 2021 GLA 250 for Air Bag Ground Connection Defect

    Mercedes-Benz is recalling 2021 GLA 250 vehicles because the front passenger air bag ground connection may be improperly mounted, risking inadvertent deployment.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ GLA 250
    Category
    Vehicle
    Distribution
    Distributed nationwide