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NA 294.52Recalls & reported problems

Synthes GmbH · 5.0MM SCHANZ SCREW BLUNTED TROCAR POINT 100MM · Class 2 · Implant

Adverse event reports
3
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10886982181497), received between Mar 17, 2021 and Mar 17, 2021 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Break” (3 reports).

5 other recalls cover devices cleared under the same FDA submission (K082650, K122455, K161417, K950384); they may or may not involve this specific model.

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

  • Break3

Patient problems

  • No Clinical Signs, Symptoms or Conditions3

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMar 17, 2021Break; Break

    IT WAS REPORTED THAT ON (B)(6) 2021, DURING AN UNKNOWN PROCEDURE, ONE (1) BROAD LOCKING COMPRESSION PLATE HOLE STRIPPED AND THE LOCKING HOLE DID NOT ENGAGE, ONE (1) BROAD LOCKING COMPRESSION PLATE BROKE AFTER EXCESSIVE BENDING, AND THE PINS OF A EIGHT (8) SHANZ SCREW BLUNTED TROCAR POINT HAD A BROKEN TIPS. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH A THREE (3) MINUTE SURGICAL DELAY. THERE WAS NO PATIENT CONSEQUENCE. THIS REPORT INVOLVES ONE (1) 5.0MM SCHANZ SCREW BLUNTED TROCAR POINT 100MM. THIS IS REPORT 7 OF 10 FOR (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11505005 ↗
  • MalfunctionMar 17, 2021Break; Break

    IT WAS REPORTED THAT ON (B)(6) 2021, DURING AN UNKNOWN PROCEDURE, ONE (1) BROAD LOCKING COMPRESSION PLATE HOLE STRIPPED AND THE LOCKING HOLE DID NOT ENGAGE, ONE (1) BROAD LOCKING COMPRESSION PLATE BROKE AFTER EXCESSIVE BENDING, AND THE PINS OF A EIGHT (8) SHANZ SCREW BLUNTED TROCAR POINT HAD A BROKEN TIPS. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH A THREE (3) MINUTE SURGICAL DELAY. THERE WAS NO PATIENT CONSEQUENCE. THIS REPORT INVOLVES ONE (1) 5.0MM SCHANZ SCREW BLUNTED TROCAR POINT 100MM. THIS IS REPORT 5 OF 10 FOR (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11504778 ↗
  • MalfunctionMar 17, 2021Break; Break

    IT WAS REPORTED THAT ON (B)(6) 2021, DURING AN UNKNOWN PROCEDURE, ONE (1) BROAD LOCKING COMPRESSION PLATE HOLE STRIPPED AND THE LOCKING HOLE DID NOT ENGAGE, ONE (1) BROAD LOCKING COMPRESSION PLATE BROKE AFTER EXCESSIVE BENDING, AND THE PINS OF A EIGHT (8) SHANZ SCREW BLUNTED TROCAR POINT HAD A BROKEN TIPS. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH A THREE (3) MINUTE SURGICAL DELAY. THERE WAS NO PATIENT CONSEQUENCE. THIS REPORT INVOLVES ONE (1) 5.0MM SCHANZ SCREW BLUNTED TROCAR POINT 100MM. THIS IS REPORT 3 OF 10 FOR (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11504717 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K082650, K122455, K161417, K950384. One submission often covers many models, so check the product and lot details in each record.

  • Z-2451-2015 · Jul 29, 2015 · Terminated
    Synthes Trauma Ex-Fix System (Small, Medium, Distraction Osteogenesis (DO) and Large) ; (S) intended to stabilize and provide treatment for fractures of the small bones, such as th
  • Z-1833-2014 · Apr 10, 2014 · Terminated
    Synthes External Fixation Systems (Small, Medium, Large and DO), bone fixation appliance components.
  • Z-0941-2013 · Jan 11, 2013 · Terminated
    Large Combination Clamp/Large External Fixation System, Part Number 390.005 Product Usage: Synthes Large External Fixation is intended for use to provide treatment for long bone
  • Z-1816-2013 · Oct 12, 2012 · Open, Classified
    Synthes Large External Fixation, MR Conditional, Tube to Tube Clamp, Part Number 390.007, Lot Number 6800599 Synthes Large External Fixation is intended for use to provide treatme
  • Z-0277-2013 · Sep 28, 2012 · Terminated
    Synthes External Fixation System Tube to Tube Clamp, Part Number 390.007. Intended for use to provide treatment for long bone and pelvic fractures that require external fixation.

Other APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE devices

All APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT, METAL COMPOSITE devices →

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