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PRECICE® Intramedullary Limb Lengthening System P10.7-80C275Recalls & reported problems

Nuvasive Specialized Orthopedics, Inc. · Orthopedic intramedullary limb lengthening rod, antegrade tibia, 10.7 mm diameter, 275 mm length · Class 2 · Implant

All models of PRECICE Intramedullary Limb Lengthening System (551)

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

2 open recalls name this device. See the recall details and contact the manufacturer or your healthcare provider.

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00812258020460), received between Dec 12, 2025 and May 27, 2026 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Failure to Advance” (2 reports).

2 FDA recall records name this device's identifier, 2 still open.

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.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 1 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 1 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Recalls naming this device

  1. Oct 29, 2021Class IIOpen, Classified

    The Instructions for Use have been updated to include: (1) Clarification that the device is intended for use only in patients 18 years and older, (2) That patients should weigh 50 lbs. or more while undergoing treatment, and (3) That no more than two devices should be implanted at a time.

    Z-0319-2022 · Root cause: Device Design · Recall details · FDA record ↗

  2. Feb 12, 2021Class IIOpen, Classified

    Due to not having the full complement of biological assessments for all potential patients and as a result the devices are not indicated for use in individuals under the age of 18 years old.

    Z-1349-2021 · Root cause: Device Design · Recall details · FDA record ↗

Most reported problems

Device problems

  • Failure to Advance2

Patient problems

  • No Clinical Signs, Symptoms or Conditions2

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionMay 27, 2026Failure to Advance

    IT WAS REPORTED THAT A PRECICE NAIL WAS IMPLANTED IN (B)(6) ON A STATURE PATIENT. HIS RIGHT SIDE LENGTHENED BUT THE LEFT NAIL DID NOT. THE PATIENT LOST FAITH IN HIS ORIGINAL SURGEON, SO HE CAME TO (B)(6) TO HAVE DR. (B)(6) SWAP OUT THE NAIL. THE NAIL DID WORK ON THE BACK TABLE WITH A FAST DISTRACTOR, BUT (B)(6) STILL WANTED US TO SWAP IT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 25306652 ↗
  • MalfunctionDec 12, 2025Failure to Advance; Failure to Advance

    IT WAS REPORTED THAT A PRECICE NAIL WAS IMPLANTED IN (B)(6) ON A STATURE PATIENT. HIS RIGHT SIDE LENGTHENED BUT THE LEFT NAIL DID NOT. THE PATIENT LOST FAITH IN HIS ORIGINAL SURGEON, SO HE CAME TO (B)(6) TO HAVE DR. (B)(6) SWAP OUT THE NAIL. THE NAIL DID WORK ON THE BACK TABLE WITH A FAST DISTRACTOR, BUT (B)(6) STILL WANTED US TO SWAP IT.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23790510 ↗

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