The Recall Desk

State

US Virgin Islands product recalls

72,936 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
30
Most recent
2026-09-09

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 30 (17%) are Severe.

These figures cover only the 177 recalls whose distribution notice names US Virgin Islands specifically. The 72,936 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

2851–2875 of 73113

  • HighNHTSA·26V137000·2026-03-11

    ARBOC Transit Buses Recalled for Rear Brake Line Installation Error

    ARBOC is recalling 2018-2026 Spirit of Freedom and Spirit of Mobility buses because incorrectly installed rear brake lines may cause the anti-lock brake system to malfunction.

    Product
    ARBOC SPECIALTY VEHICLES — ARBOC SPECIALTY VEHICLES SPIRIT OF FREEDOM, SPIRIT OF MOBILITY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1491-2026·2026-03-11

    Stago free protein S assay may underestimate normal range results

    Diagnostica Stago is recalling four lots of the STA Liatest Free Protein S kit because of the potential for out-of-range results and underestimation of free protein S in normal patient plasmas.

    Product
    Brand Name: STA Liatest Free Protein S Product Name: STA Liatest Free Protein S Model/Catalog Number (REF): 00516 Product Description: The STA¿ - Liatest¿ Free Protein S kits are intended for use on STA-R¿ and STA Compact¿ for the quantitative antigenic assay of free protein S
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1483-2026·2026-03-11

    B. Braun 21GA winged infusion sets may have blunt needle tips

    B. Braun Medical is recalling 21GA Winged Infusion Sets, model 7M2802, because the needle tip may be dull or blunt, difficult to advance, or may break.

    Product
    Brand Name: B. Braun Product Name: 21GA WINGED INF SET Model/Catalog Number: 7M2802 Software Version: N/A Product Description: A device designed for subcutaneous implantation and intended to be used temporarily to expand an implanted tissue expander by percutaneous injection
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1490-2026·2026-03-11

    Esaote endocavity ultrasound probe recalled because liquid may leak in

    Esaote is recalling five Endocavity ultrasonic probes, model E 3-12, because a potential weakness in the probe body may allow liquid to leak from the casing near the cable.

    Product
    Esaote Endocavity ultrasonic probe, Model E 3-12, REF 120000038
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1489-2026·2026-03-11

    Olympus biopsy valve MAJ-1218 may shed rubber fragments during use

    Olympus is recalling all lots of its Single Use Biopsy Valve, model MAJ-1218, because of the potential for rubber fragment detachment during use.

    Product
    Olympus Single Use Biopsy Valve. Model/Catalog Number: MAJ-1218. 20 units per box. The MAJ-1218 has been designed to be attached to the instrument channel port of compatible endoscopes to prevent leakage of body fluids.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • HighNHTSA·26V136000·2026-03-11

    Volvo EX30 seat belt warning chime may not sound as intended

    Volvo is recalling certain 2025-2026 EX30 and 2026 EX30CC vehicles because the seat belt warning system may not activate the audible warning chime. This fails FMVSS 208.

    Product
    VOLVO — VOLVO EX30CC, EX30
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·26V138000·2026-03-11

    2025–2026 Volkswagen Jetta Vehicles Recalled for Transmission Ground Wire

    Volkswagen is recalling certain 2025–2026 Jetta vehicles because the transmission ground wire may not have been properly connected during assembly, creating an open electrical circuit that could increase fire risk.

    Product
    VOLKSWAGEN — VOLKSWAGEN JETTA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Drugs)·D-0389-2026·2026-03-11

    Sodium iodide I-131 oral solution recalled over particulate matter

    Radnostix is recalling one batch of Sodium Iodide I-131 Therapeutic Oral Solution because of the presence of particulate matter caused by production issues.

    Product
    SODIUM IODIDE I-131 — SODIUM IODIDE I-131 (SODIUM IODIDE I-131)
    Category
    Drug
    Distribution
    Distributed nationwide
  • HighFDA (Devices)·Z-1484-2026·2026-03-11

    Siemens urine albumin assay may report falsely depressed patient results

    Siemens Healthcare Diagnostics is recalling all lots of the Atellica CH Urine Albumin assay because falsely depressed patient results may occur above the measuring interval.

    Product
    Atellica CH Urine Albumin (UAlb). Material Number: 11537225
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0385-2026·2026-03-11

    Vasocaine lidocaine spray recalled because stability data does not support expiry

    HTO Nevada, trading as Kirkman, is recalling Five-Star Vasocaine Spray because the stability data does not support the labeled expiry date.

    Product
    FIVE-STAR, VASOCAINE Spray, (Lidocaine HCl 4%, Racepinephrine HCl 0.01%), 4oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-016.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0387-2026·2026-03-11

    Zone 2 lidocaine cream recalled because stability data does not support expiry

    HTO Nevada, trading as Kirkman, is recalling one lot of Maximum Zone 2 4% Lidocaine Cream because the stability data does not support the labeled expiry date.

    Product
    MAXIMUM, ZONE 2, 4% Lidocaine Cream, (Lidocaine 4% and Epinephrine 0.01%), 1 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-015.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Devices)·Z-1486-2026·2026-03-11

    Datascope CS100 balloon pump manual recalled for outdated battery specifications

    Datascope is recalling the CS100 IABP running software version Q.01 because the battery runtime and cycle specifications in the device's Instructions for Use need to be updated.

    Product
    CS100 IABP. Software Version CS100 IABP Q.01.
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0386-2026·2026-03-11

    Zone 1 lidocaine cream recalled because stability data does not support expiry

    HTO Nevada, trading as Kirkman, is recalling one lot of Maximum Zone 1 4% Lidocaine Cream because the stability data does not support the labeled expiry date.

    Product
    MAXIMUM, ZONE 1, 4% Lidocaine Cream, 1/2 oz bottles, Distributed By: Dermal Source, Portland, OR 97232, NDC 80069-014.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0365-2026·2026-03-11

    Medi-First antiseptic wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Medi-First Antiseptic Wipes over current good manufacturing practice deviations.

    Product
    MEDI-FIRST ANTISEPTIC WIPES — MEDI-FIRST ANTISEPTIC WIPES (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0372-2026·2026-03-11

    WipesPlus hand sanitizing wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling WP WipesPlus Hand Sanitizing Wipes over current good manufacturing practice deviations.

    Product
    WP WipesPlus Hand Sanitizing Wipes (Benzalkonium Chloride 0.13%), 5x7, 100 CT, Progressive Products, 211 S. Ridge Street, Rye Brook, NY 10573. NDC 67151-727-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0364-2026·2026-03-11

    Savannah antibacterial towelettes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Savannah Antibacterial Towelettes over current good manufacturing practice deviations.

    Product
    Savannah Antibacterial Towelettes (Benzalkonium Chloride 0.13%), 1 towelette, 4 x 7, R&R Enterprise, NDC 59647-749-02
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0368-2026·2026-03-11

    WipesPlus alcohol free BZK wipes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Wipes Plus Hand Sanitizing Alcohol Free BZK Wipes over current good manufacturing practice deviations.

    Product
    Wipes Plus, Hand Sanitizing Alcohol Free BZK Wipes (Benzalkonium Chloride 0.13%), Manufactured for: CFS Brands DBA WipesPlus, 4711 E. Heiner Rd. Oklahoma City, OK 73331, NDC 67151-333-01.
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0366-2026·2026-03-11

    Med-Nap BZK antiseptic towelettes recalled over manufacturing practice deviations

    Acme United Corporation is recalling Med Nap BZK Antiseptic Towelettes in 100-count packs over current good manufacturing practice deviations.

    Product
    MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC — MED NAP BENZALKONIUM CHLORIDE ANTISEPTIC (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide
  • ModerateFDA (Drugs)·D-0359-2026·2026-03-11

    First Aid Only BZK antiseptic towelettes recalled over manufacturing deviations

    Acme United Corporation is recalling First Aid Only BZK Antiseptic Towelettes over current good manufacturing practice deviations.

    Product
    FIRST AID ONLY BZK ANTISEPTIC — FIRST AID ONLY BZK ANTISEPTIC (BENZALKONIUM CHLORIDE)
    Category
    Drug
    Distribution
    Distributed nationwide