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WECK IPN028499Recalls & reported problems

Teleflex Incorporated · RANEY CLIPS DISPOSABLE 10/pouch · Class 2

Adverse event reports
2
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 34026704631811), received between Jul 27, 2021 and Mar 30, 2022 — classified as 1 injury, 1 malfunction.

The most frequently reported specific device problem is “Break” (2 reports).

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

  • Break2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2
  • Foreign Body In Patient1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 30, 2022Break; Break

    FAILURE DESCRIPTION: WHEN APPLYING RANEY CLIP IT BROKE INTO SEVERAL PIECES. 2 LARGE PIECES WERE RECOVERED AND 1 SMALL PIECE. HOWEVER, THERE WAS 1 PIECE THAT WAS NOT FOUND. THE SURGICAL FIELD WAS SEARCHED AS WELL AS THE FLOOR OF THE OR. THE IRRIGATION POUCH WAS SUCTIONED OUT AS WELL. EVENT OCCURRED WHEN I WAS AT AN EDUCATIONAL MEETING SO, THIS WAS RELAYED TO ME BY ANOTHER RN. MANAGEMENT WAS PAGED FOR FURTHER GUIDANCE.

    Patient problems: Foreign Body In Patient; No Clinical Signs, Symptoms or Conditions

    MAUDE report 13957539 ↗
  • MalfunctionJul 27, 2021Break; Break

    THE CLIPS SHATTERED DURING PROCEDURE. NO SAMPLE AVAILABLE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12226377 ↗

Other CLIP, SCALP devices

All CLIP, SCALP devices →

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