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SKYLINE 186862018Recalls & reported problems

Medos International Sàrl · SKYLINE ANTERIOR CERVICAL PLATE SYSTEM CONSTRAINED SELF-TAPPING SCREW 4 x 18mm · Class 2 · Implant

All models of SKYLINE (39)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705034134642), received between Jul 27, 2022 and Jul 27, 2022 — classified as 1 injury.

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

7 other recalls cover devices cleared under the same FDA submission (K052552, K171439); 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Migration1

Patient problems

  • Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
  • Unspecified Tissue Injury1

Recent adverse event reports

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

  • InjuryJul 27, 2022Migration; Migration

    IT WAS REPORTED THAT ON AN UNKNOWN DATE THE PATIENT HAD A C56 ACDF ON (B)(6) 2022 USING SKYLINE AND VG2 ALLOGRAFT. POST OPERATIVELY THE PATIENT FELL DOWN THE STAIRS DISRUPTING THE IMPLANTS WHICH RESULTED IN THE LEFT C6 SCREW MIGRATING ANTERIORLY FROM THE PLATE. A REVISION SURGERY WAS COMPLETED TO REPLACE THE PLATE AND SCREWS. THE PATIENT REQUIRED A REVISION SURGERY DUE TO THE MIGRATION OF THE SCREW ANTERIORLY. THERE WAS A CLINICAL OUTCOME EXPERIENCED BY THE PATIENT BECAUSE A REVISION SURGERY WAS DONE DUE TO THE MIGRATION OF THE SCREW ANTERIORLY. THERE IS NO FURTHER INFORMATION. THIS REPORT IS FOR ONE (1) SKY CONST S-T SCW 18MM TI. THIS IS REPORT 3 OF 5 FOR COMPLAINT (B)(4).

    Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available; Unspecified Tissue Injury

    MAUDE report 15114515 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K052552, K171439. One submission often covers many models, so check the product and lot details in each record.

  • Z-0630-2017 · Oct 12, 2016 · Terminated
    DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM CONSTRAINED OVERSIZED SCREW 4.5 x 18mm Item Code: 186864018 The SKYLINE Anterior Cervical Plate System is indicated for stabil
  • Z-0628-2017 · Oct 12, 2016 · Terminated
    DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE OVERSIZED SCREW 4.5 x 18mm Item Code: 186854018 The SKYLINE Anterior Cervical Plate System is indicated for stabilizat
  • Z-0627-2017 · Oct 12, 2016 · Terminated
    DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING SCREW 4.0 x 26mm Item Code: 186852026 The SKYLINE Anterior Cervical Plate System is indicated for stabili
  • Z-0625-2017 · Oct 12, 2016 · Terminated
    DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING SCREW 4.0 x 18mm Item Code: 186852018 The SKYLINE Anterior Cervical Plate System is indicated for stabi
  • Z-0626-2017 · Oct 12, 2016 · Terminated
    DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-TAPPING SCREW 4.0 x 20mm Item Code: 186852020 The SKYLINE Anterior Cervical Plate System is indicated for stabiliz
  • Z-0624-2017 · Oct 12, 2016 · Terminated
    DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM VARIABLE SELF-DRILLING SCREW 4.0 x 18mm Item Code: 186850018 The SKYLINE Anterior Cervical Plate System is indicated for stabi
  • Z-0629-2017 · Oct 12, 2016 · Terminated
    DePuy Spine SKYLINE ANTERIOR CERVICAL PLATE SYSTEM CONSTRAINED SELF-TAPPING SCREW 4 x 18mm Item Code: 186862018 The SKYLINE Anterior Cervical Plate System is indicated for stabi

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Sources and updates

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