Facility

STIHLER ELECTRONIC GMBH

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

Key facts

1recalls · worst Class II

—inspections in our data

—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)	3001733054
Establishment type	Manufacture Medical Device
Location	Gaussstrasse 4 Leinfelden-Echterdingen Baden-Wurttemberg, DE 70771
Registration status	Active · expires 2026
Parent company	STIHLER ELECTRONIC GMBH (owner-operator 9036252)
Brand names	Astoflo Plus ECO; Astoflo Plus

Activity by year

Recalls (1)

Devices registered here (1)

Warmer, Thermal, Infusion Fluid
Product code LGZ (opens in a new tab) · Class II · General Hospital · 21 CFR 880.5725

Recalls & enforcement

Class IITerminated2018-09-06
PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control Unit, damage may result in a hotspot on the Heating Profile, may cause low level skin burn

All facilities operated by STIHLER ELECTRONIC GMBH

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. “STIHLER ELECTRONIC GMBH (FEI 3001733054) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3001733054-stihler-electronic-gmbh/

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