PRECICE® STRYDE System PS10.0-50D235Recalls & reported problems
Nuvasive Specialized Orthopedics, Inc. · Antegrade Femur Trochanter 10° Bend · Class 2 · Implant
All models of PRECICE STRYDE System (231)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 7
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 00887517951168), received between Feb 25, 2020 and Jun 13, 2022 — classified as 2 injuries, 5 malfunctions.
The most frequently reported specific device problem is “Break” (3 reports).
1 FDA recall record name this device's identifier, 1 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 16, 2026.
Recalls naming this device
- Feb 12, 2021Open, 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 ↗
Most reported problems
Device problems
- Break3
- Corroded2
- Failure to Advance1
- Fracture1
Patient problems
- Failure of Implant4
- No Clinical Signs, Symptoms or Conditions2
- Foreign Body In Patient1
Recent adverse event reports
The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 13, 2022Break; Break
INFORMATION WAS RECEIVED THAT DURING REMOVAL, THE NAIL WAS BROKEN AND A PORTION OF THE NAIL REMAINED IN THE PATIENT'S FEMUR DESPITE MULTIPLE ATTEMPTS TO EXTRACT IT. NO PATIENT OR USER HARM OR ADVERSE IMPACT WAS REPORTED.
Patient problems: Foreign Body In Patient
MAUDE report 14682164 ↗MalfunctionDec 28, 2021Corroded; Corroded
NO ADDITIONAL INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13102042 ↗MalfunctionAug 17, 2021Break; Break
InjuryApr 19, 2021Fracture; Fracture
MalfunctionMar 30, 2021Corroded; Corroded
NO ADDITIONAL INFORMATION HAS BEEN PROVIDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11589362 ↗InjuryJun 18, 2020Break; Break
INFORMATION WAS RECEIVED THAT X-RAY IMAGES REVEALED THAT THE NAIL BROKE AT THE DISTAL PROXIMAL SCREW. AS PER THE REPORTER, THE PATIENT EXPERIENCED PAIN IN (B)(6) 2019. IT IS UNKNOWN IF A REVISION PROCEDURE IS PLANNED.
Patient problems: Failure of Implant
MAUDE report 10171127 ↗MalfunctionFeb 25, 2020Failure to Advance; Failure to Advance
INFORMATION WAS RECEIVED THAT A REVISION PROCEDURE WAS PERFORMED ON (B)(6) 2020. AS PER THE REPORTER THE NAIL FAILED TO LENGTHEN.
Patient problems: Failure of Implant
MAUDE report 9751914 ↗
Other Rod, Fixation, Intramedullary And Accessories devices
- NA 03.033.001Synthes GmbH · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES265 reports
- GAMMA 3125-1180SStryker GmbH · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES249 reports
- NA 03.037.026Synthes GmbH · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES225 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-075Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls2 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-045Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls1 report
- TRIGEN 71674067Smith & Nephew, Inc. · ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES201 reports
- PRECICE® Intramedullary Limb Lengthening System LSC5-050Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls1 report
- PRECICE Intramedullary Limb Lengthening System LSB5-075Nuvasive Specialized Orthopedics, Inc. · Rod, Fixation, Intramedullary And Accessories4 recalls0 reports
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 · each recall links to the FDA recall notice
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
How reports and recalls are matched · Editorial policy · Report an error on this page