RegWardenFDA facility compliance records
Facility

SHEATHING TECHNOLOGIES, INC.

1 recall(s) on record — most severe on record: Class II.

Activity by year

FDA actions on record by year2016: 1 inspections; 2023: 1 inspections; 2025: 1 recalls12016201720182019202020212022120232024120252026
  • Recalls (1)
  • Inspections (2)

Devices registered here (1)

Recalls & enforcement

  • Class IIOngoing2025-11-17
    Vaginal/rectal ultrasound probe covers with a viral barrier may have product defects, which may result in contamination during use, posing an infection risk.

FDA inspections (2)

  • NAI2023-08-02
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices
  • NAI2016-03-02
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices

Source: U.S. FDA Inspections Dashboard (opens in a new tab) (device inspection classifications, 2016–present). Data as of 2026-10-06. The dashboard profile can take several seconds to load.

Related

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this facility record at FDA → (opens in a new tab)

Cite this record

RegWarden. “SHEATHING TECHNOLOGIES, INC. (FEI 1000135740) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/1000135740-sheathing-technologies-inc/

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