RegWardenFDA facility compliance records
Company

PETER LAZIC GMBH

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

Recalls by year

FDA actions on record by year2023: 2 recalls20172018201920202021202222023202420252026
  • Recalls (2)

Registered facilities (1)

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.

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. We restate the public record only — measured facts, never risk verdicts.

Cite this record

RegWarden. “PETER LAZIC GMBH — FDA compliance profile.” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/company/oo-8010890-peter-lazic-gmbh/

Not open yet

Alerts for PETER LAZIC 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.