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The Locking Pediatric Osteotomy Plate (LolliPOP) System POP-M3IRecalls & reported problems

Orthopediatrics Canada ULC · M3 Connector For Infant · Class 2 · Implant

Data updated Oct 18, 2026 from official FDA records · Editorial policy

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 07540194006691), received between Sep 30, 2022 and Sep 30, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Detachment of Device or Device Component” (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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Detachment of Device or Device Component1
  • Material Separation1

Patient problems

  • Malunion of Bone1

Recent adverse event reports

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

  • MalfunctionSep 30, 2022Material Separation; Detachment of Device or Device Component; Material Separation; Detachment of Device or Device Component

    INFANT BLADE AND PLATE IMPLANTED THREE WEEKS AGO, DETACHED IN THE PATIENT. THE CONNECTOR THAT FIXED THE BLADE AND PLATE GOT LOOSENED.

    Patient problems: Malunion of Bone

    MAUDE report 15510780 ↗

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

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

Sources and updates

How reports and recalls are matched · Editorial policy · Report an error on this page