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SKYLINE 186860017Recalls & reported problems

Medos International Sàrl · SKYLINE ANTERIOR CERVICAL PLATE SYSTEM CONSTRAINED SELF-DRILLING SCREW 4 x 17mm · 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 10705034134529), received between Dec 28, 2020 and Dec 28, 2020 — 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

  • Failure of Implant1

Recent adverse event reports

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

  • InjuryDec 28, 2020Migration; Migration

    DEVICE REPORT FROM (B)(6) REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT ON AN UNKNOWN DATE, DURING THE FOLLOW-UP, THE SURGEON DISCOVERED THAT ONE OF THE SCREWS HAS BEEN PULLED OUT. THE PATIENT HAD AN ACDF SURGERY USING A SKYLINE PLATE ON (B)(6) 2020. IT WAS UNKNOWN THAT THE PATIENT IF SCHEDULE FOR FURTHER PROCEDURE. THE PATIENT OUTCOME WAS UNKNOWN. CONCOMITANT MEDICAL PRODUCTS: SKYLINE PLATE (PART# UNKNOWN, LOT# UNKNOWN, QUANTITY UNKNOWN). THIS COMPLAINT INVOLVES ONE DEVICE. THIS REPORT IS FOR ONE (B)(4). THIS REPORT IS ONE OF ONE FOR (B)(4).

    Patient problems: Failure of Implant

    MAUDE report 11081913 ↗

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-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-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-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-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

Other APPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY devices

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Sources and updates

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