Facility

SCHILLER AG

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

Key facts

2recalls · worst Class II

1inspections · worst VAI

—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)	3002808182
Establishment type	Manufacture Medical Device
Location	ALTGASSE 68 BAAR Zug, CH 6341
Registration status	Active · expires 2026
Parent company	SCHILLER AG (owner-operator 8030978)
Brand names	Thermal paper

Activity by year

Recalls (2)
Inspections (1)

Devices registered here (1)

Recorder, Paper Chart
Product code DSF (opens in a new tab) · Class I · Cardiovascular · 21 CFR 870.2810

Recalls & enforcement

Class IIOngoing2025-08-08
Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.
Class IIOngoing2024-07-24
Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.

FDA inspections (1)

VAI2024-01-25
Voluntary 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.

All facilities operated by SCHILLER AG

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. “SCHILLER AG (FEI 3002808182) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3002808182-schiller-ag/

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