Skip to content

AESCULAP PL512RRecalls & reported problems

Aesculap AG · CHALLENGER TI Clip Applier Forceps, multi-fire, (310 mm), diam. 5 mm, consisting of PL510R, PL522R, reusable, reposable, to be usedwith: PL572T · Class 1

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 04038653208456), received between Jun 29, 2021 and Jun 29, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Ejection Problem” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Ejection Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionJun 29, 2021Ejection Problem; Ejection Problem

    ADDITIONAL INFORMATION: INVOLVED COMPONENTS PL522R - SHAFT COMPL.D:5MM L:310MM - LOT UNKNOWN.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12085541 ↗

Other Applier, surgical, clip devices

All Applier, surgical, clip devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.