RegWardenFDA facility compliance records
Facility

KARL STORZ SE & CO. KG

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

Activity by year

FDA actions on record by year2016: 1 recalls120162017201820192020202120222023202420252026
  • Recalls (1)

Devices registered here (4)

  • Forceps, Biopsy, Electric
    Product code KGE (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.4300
  • Dissector, Surgical, General & Plastic Surgery
    Product code GDI (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4800
  • Snare, Flexible
    Product code FDI (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.4300
  • Unit, Electrosurgical, Endoscopic (With Or Without Accessories)
    Product code KNS (opens in a new tab) · Class II · Gastroenterology, Urology · 21 CFR 876.4300

Recalls & enforcement

  • Class IITerminated2016-02-29
    Endoscope cleaning brush 11276CL may not fit resulting in an inability to insert the brush in to the channel of the intended endoscope or to completely pass it through such channel.

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. “KARL STORZ SE & CO. KG (FEI 3006546082) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3006546082-karl-storz-se-co-kg/

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