Facility

PETER LAZIC GMBH

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

Key facts

2recalls · 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)	3007264034
Establishment type	Manufacture Medical Device
Location	Immelmannweg 2 TUTTLINGEN Baden-Wurttemberg, DE 78532
Registration status	Active · expires 2026
Parent company	PETER LAZIC GMBH (owner-operator 8010890)

Activity by year

Recalls (2)

Devices registered here (1)

Hook, Surgical, General & Plastic Surgery
Product code GDG (opens in a new tab) · Class I · General, Plastic Surgery · 21 CFR 878.4800

Recalls & enforcement

Class IIOngoing2023-10-06
Customer complaint received that reported the applier failed during surgery. The applier did not release the clip. The applier remained attached to the clip.
Class IIOngoing2023-07-14
Wrong product coloring. The paddle clips should be blank, but they are colored blue.

All facilities operated by PETER LAZIC 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. “PETER LAZIC GMBH (FEI 3007264034) — FDA facility record.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/facility/3007264034-peter-lazic-gmbh/

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