Facility

MUNEVO 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)	3021337381
Establishment type	Complaint File Establishment per 21 CFR 820.198; Manufacture Medical Device
Location	Agnes-pockels-bogen 1 Munich Bavaria, DE 80992
Registration status	Active · expires 2026
Parent company	Munevo GmBH (owner-operator 10083888)
Brand names	munevo DRIVE

Activity by year

Recalls (1)

Devices registered here (1)

Components, Wheelchair
Product code KNN (opens in a new tab) · Class I · Physical Medicine · 21 CFR 890.3920

Recalls & enforcement

Class IIOngoing2026-06-19
A software issue may cause the wheelchair's driving mechanism to fall out of calibration. When this occurs, the device may experience unexpected steering drift or imprecise control while driving the wheelchair. The wheelchair may veer from its intended path, which may cause in lo…

All facilities operated by Munevo 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. “MUNEVO GMBH (FEI 3021337381) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3021337381-munevo-gmbh/

Not open yet

Alerts for MUNEVO GMBH

Watchlist alerts will email you when FDA publishes a new recall, inspection classification, or warning letter for a facility you follow. They aren't open to the public yet — leave your email and we'll tell you when they are.

Planned

Want a one-page facility brief?

A single-page summary of this facility's registration and recall history for diligence. Not selling it yet — register interest and we'll follow up.