Facility

HAGER & MEISINGER GMBH

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

Key facts

2recalls · 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)	3004169071
Establishment type	Manufacture Medical Device
Location	HANSEMANNSTRASSE 10 NEUSS North Rhine-Westphalia, DE 41468
Registration status	Active · expires 2026
Parent company	HAGER & MEISINGER GMBH (owner-operator 8010516)

Activity by year

Recalls (2)
Inspections (1)

Devices registered here (1)

Burr, Orthopedic
Product code HTT (opens in a new tab) · Class I · Orthopedic · 21 CFR 888.4540

Recalls & enforcement

Class IITerminated2020-07-15
US-dates between the product package label and the bar code display.
Class IIOngoing2018-11-07
Incorrect packaging; There is a potential that a 1.0 mm carbide blade was packaged in a 0.9 mm carbide blade packaging.

FDA inspections (1)

NAI2017-09-07
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.

All facilities operated by HAGER & MEISINGER 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. “HAGER & MEISINGER GMBH (FEI 3004169071) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3004169071-hager-meisinger-gmbh/

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