RegWardenFDA facility compliance records
Facility

TROKAMED GMBH

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

Activity by year

FDA actions on record by year2016: 1 inspections; 2024: 1 recalls1201620172018201920202021202220231202420252026
  • Recalls (1)
  • Inspections (1)

Devices registered here (1)

  • Laparoscope, General & Plastic Surgery
    Product code GCJ (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.1500

Recalls & enforcement

  • Class IOngoing2024-11-27
    If the inflow speed is too quick, it could result in reduced outflow through the shaft due to blood, tissue fragments and kidney stone fragments, and quickly build up of intrarenal pressure.

FDA inspections (1)

  • NAI2016-02-19
    No Action Indicated · Compliance: Devices; Postmarket Assurance: Devices · citations posted

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. “TROKAMED GMBH (FEI 3004595684) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3004595684-trokamed-gmbh/

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