OrthoPediatrics PediNail Intramedullary Nailing System 10-1500-043Recalls & reported problems
Orthopediatrics Corp. · IM FEMORAL NAIL, 9mm x 32cm, Right · Class 2 · Implant
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841132118832), received between Aug 8, 2025 and Aug 8, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fracture” (1 report).
27 other recalls cover devices cleared under the same FDA submission (K083726); they may or may not involve this specific model.
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
Most reported problems
Device problems
- Fracture1
Patient problems
- Failure of Implant1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 8, 2025Fracture; Fracture
THE PATIENT BROKE HIS PEDINAIL WITHIN TWO MONTHS TIME.
Patient problems: Failure of Implant
MAUDE report 22764512 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K083726. One submission often covers many models, so check the product and lot details in each record.
- Z-0879-2017 · Nov 18, 2016 · TerminatedOrthoPediatrics PediNail Intramedullary Nailing System 4.5mm X 48mm Cortical Screw
- Z-0339-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 7mm x 20 cm, Rt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-021. The system is used for pediatric and small stature adult patients
- Z-0360-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 8mm x 28 cm, Lt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-083. The system is used for pediatric and small stature adult patients
- Z-0351-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 8mm x 36 cm, Rt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-037. The system is used for pediatric and small stature adult patients
- Z-0342-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 7mm x 26 cm, Rt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-024. The system is used for pediatric and small stature adult patients
- Z-0358-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 8mm x 24 cm, Lt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-081. The system is used for pediatric and small stature adult patients
- Z-0355-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 7mm x 26 cm, Lt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-074. The system is used for pediatric and small stature adult patients
- Z-0359-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 8mm x 26 cm, Lt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-082. The system is used for pediatric and small stature adult patients
- Z-0354-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 7mm x 24 cm, Lt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-073. The system is used for pediatric and small stature adult patients
- Z-0361-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 8mm x 30 cm, Lt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-084. The system is used for pediatric and small stature adult patients
- Z-0341-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 7mm x 24 cm, Rt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-023. The system is used for pediatric and small stature adult patients
- Z-0364-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 8mm x 36 cm, Lt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-087. The system is used for pediatric and small stature adult patients
- Z-0352-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 7mm x 20 cm, Lt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-071. The system is used for pediatric and small stature adult patients
- Z-0348-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 8mm x 30 cm, Rt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-034. The system is used for pediatric and small stature adult patients
- Z-0357-2010 · Jul 21, 2009 · TerminatedOrthopediatrics IM Femoral Nail - 7mm x 30 cm, Lt, non-sterile, Orthopediatrics, Warsaw, IN; Part # 10-1500-076. The system is used for pediatric and small stature adult patients
…and 12 more.
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
- PRECICE® Intramedullary Limb Lengthening System LSC5-050Nuvasive 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 LSB5-040Nuvasive 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
- 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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