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PRECICE® Bone Transport System BT10-90SJ340-7Recalls & reported problems

Nuvasive Specialized Orthopedics, Inc. · Antegrade Tibia 10° Bend – Three Holes, 10.0mm x 340mm, 7/9cm ST · Class 2 · Implant

All models of PRECICE Bone Transport System (561)

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
1
Deaths reported
0
Injuries reported
0
Recalls naming it
2

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00887517979780), received between Mar 29, 2022 and Mar 29, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (1 report).

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.

Recalls naming this device

  1. Feb 12, 2021Class IIOpen, Classified

    Due to complaints of adverse events potentially related to biological safety. The complaints included report of pain and bony abnormalities at the interface between the telescoping nail segments.

    Z-1323-2021 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

  2. Feb 12, 2021Class IIOpen, Classified

    Due to complaints of adverse events potentially related to biological safety. The complaints included report of pain and bony abnormalities at the interface between the telescoping nail segments.

    Z-1324-2021 · Root cause: Under Investigation by firm · Recall details · FDA record ↗

Most reported problems

Device problems

  • Fracture1
  • Off-Label Use1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

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

  • MalfunctionMar 29, 2022Fracture; Off-Label Use; Fracture; Off-Label Use

    INFORMATION WAS RECEIVED THAT WHILE RETRACTING THE NAIL TO SEE IF IT STILL WORKED, IT WAS NOTED ON THE INTRA-OPERATIVE X-RAYS, THAT THE NAIL WAS BROKEN INTO TWO SEGMENTS. THE NAIL WAS STILL FUNCTIONAL, AND THE SURGEON OPTED TO RETRACT THE NAIL AND LEAVE IT IN-SITU TO CONTINUE BONE TRANSPORT OF THE PATIENT'S FEMUR. NO PATIENT ADVERSE EVENT WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13938754 ↗

Other Rod, Fixation, Intramedullary And Accessories devices

All Rod, Fixation, Intramedullary And Accessories devices →

Sources and updates

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