GAP ENDO-EXO MEDULLARY SYSTEM GAP-N56-28Recalls & reported problems
Orthopediatrics Canada ULC · Nail Ø5.6mm X 280mm · Class 2 · Implant
Data updated Oct 18, 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 07540194000866), received between Jul 23, 2021 and Jul 23, 2021 — classified as 1 injury.
The most frequently reported specific device problem is “Fracture” (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
- Fracture1
Patient problems
- Bone Fracture(s)1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 23, 2021Fracture; Fracture
ON (B)(6) 2021, THE GAP ENDO-EXO MEDULLARY SYSTEM NAIL GAP-56-28 WAS IMPLANTED IN THE TIBIA OF A PATIENT WITH CONGENITAL TIBIAL PSEUDOARTHROSIS. THE NAIL WAS REPORTED BROKEN ON (B)(6) 2021, 10 WEEKS AND FOUR DAYS AFTER IMPLANTATION.
Patient problems: Bone Fracture(s)
MAUDE report 12218708 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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