Skip to content

PRECICE® Intramedullary Limb Lengthening System ERC 2Recalls & reported problems

Nuvasive Specialized Orthopedics, Inc. · ERC2, MAGEC, Shipping Pkg EU · Class 2

All models of PRECICE Intramedullary Limb Lengthening System (551)

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 00812258022860), received between Jun 11, 2020 and Jun 11, 2020 — classified as 1 injury.

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

  • Appropriate Device Problem Term/Code Not Available1

Patient problems

  • Burn(s)1

Recent adverse event reports

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

  • InjuryJun 11, 2020Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available

    INFORMATION WAS RECEIVED THAT A PATIENT HAD SUFFERED A BURN WITH THE ELECTRONIC REMOTE CONTROLLER (ERC). AS PER THE SURGEON, THE SKIN WAS A BIT RED AFTER THE DISTRACTION SESSION. REPORTEDLY, IMAGES PROVIDED BY THE MOTHER REVEALED A BURN ON THE SKIN AND CLEAR LIQUID COMING OUT OF THE AFFECT AREA. THE SURGEON PRESCRIBED ANTIBIOTIC AND A PICO MEDICAL DEVICE.

    Patient problems: Burn(s)

    MAUDE report 10146667 ↗

Other Rod, Fixation, Intramedullary And Accessories devices

All Rod, Fixation, Intramedullary And Accessories devices →

Sources and updates

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