Facility

STORZ ENDOSKOP PRODUKTIONS GMBH

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

Key facts

1recalls · worst Class II

1inspections · worst NAI

—warning letters in our data

Recalls are listed for the parent company: openFDA recall records do not name a facility. How we attribute records

FDA Establishment Identifier (FEI)	3002808273
Establishment type	Manufacture Medical Device for Another Party (Contract Manufacturer)
Location	SCHNECKENACKERSTRASSE 1 SCHAFFHAUSEN, CH CH-8200
Registration status	Active · expires 2026
Parent company	KARL STORZ SE & CO KG (owner-operator 8010119)
Brand names	ARTHROPUMP Plus

Activity by year

Recalls (1)
Inspections (1)

Devices registered here (1)

Arthroscope
Product code HRX (opens in a new tab) · Class II · Orthopedic · 21 CFR 888.1100

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.

FDA inspections (1)

NAI2022-09-29
No Action Indicated · Compliance: 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.

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. “STORZ ENDOSKOP PRODUKTIONS GMBH (FEI 3002808273) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3002808273-storz-endoskop-produktions-gmbh/

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