Facility

HENRY SCHEIN SERVICES 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)	3009142030
Establishment type	Export Device to the United States But Perform No Other Operation on Device
Location	Am Heisterbusch 9 Gallin Mecklenburg-Western Pomerania, DE 19258
Registration status	Active · expires 2026
Parent company	HENRY SCHEIN, INC. (owner-operator 2411236)
Brand names	SCISSORS, ORTHOPEDIC, SURGICAL

Activity by year

Recalls (1)

Devices registered here (1)

Scissors, Orthopedic, Surgical
Product code HRR (opens in a new tab) · Class I · Orthopedic · 21 CFR 888.4540

Recalls & enforcement

Class IIOngoing2026-07-09
Specific lots were distributed in the US with incorrect packaging and Instructions for Use (IFU) from the U.S. FDA-cleared device.

All facilities operated by HENRY SCHEIN, INC.

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. “HENRY SCHEIN SERVICES GMBH (FEI 3009142030) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3009142030-henry-schein-services-gmbh/

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