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PROACCESS 03.612.003Recalls & reported problems

Synthes GmbH · PROACCESS(TM) TABLE CLAMP · 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 10705034714479), received between Dec 4, 2020 and Dec 4, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Compatibility 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

  • Compatibility 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.

  • MalfunctionDec 4, 2020Compatibility Problem; Compatibility Problem

    IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE MIS SUPPORT SYSTEM BED ATTACHMENT NO LONGER TIGHTENS SUFFICIENTLY TO THE BED. ACTION TAKEN WHEN THE EVENT OCCURRED IS OPENED THE SECOND SET OF INSTRUMENTS. THERE WAS A SURGICAL DELAY OF 5 MINUTES. THE PROCEDURE WAS SUCCESSFULLY COMPLETED. THE PATIENT OUTCOME WAS UNKNOWN. THIS REPORT IS FOR 1 PROACCESS(TM) TABLE CLAMP. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 10945646 ↗

Other RETRACTOR devices

All RETRACTOR devices →

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