LCP 02.108.343Recalls & reported problems
Synthes GmbH · PEDIATRIC LCP HIP PLATE 5.0MM/130°/9 HOLES · Class 2 · Implant
All models of LCP (367)
Data updated Oct 16, 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 10886982029997), received between Apr 29, 2022 and Apr 29, 2022 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (1 report).
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.
Most reported problems
Device problems
- Break1
Patient problems
- Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryApr 29, 2022Break; Break
IT WAS REPORTED ON (B)(6) 2022 THAT A PATIENT HAD A HISTORY OF EWING SARCOMA OF THE RIGHT FEMUR. THERE WAS APPROXIMATE 20CM BONE DEFECT FROM A NON-UNION AFTER RESECTION OF THE SARCOMA. THE BROKEN PLATE AND ALL SCREWS AND APPROXIMATED 20CM CEMENT SPACER WERE REMOVED. THE FEMUR WAS REAMED WITH A 11MM RIA2 HEAD AND FINISHED REAMING WITH A 11.5MM STANDARD REAMER AND ALSO INSERTED A 10MM TI CANN FRN/GT 340MM RIGHT FEMORAL NAIL. THE NAIL LOCKED PROXIMALLY WITH 2 EACH RECON SCREWS AND DISTALLY WITH 2 EACH 5.0 LOCKING SCREWS. THE PLATE WAS ORIGINALLY IMPLANTED ABOUT 6 WEEKS AGO AND BROKE WHILE THE PATIENT WAS TRANSFERRING TO A CHAIR. THE PROCEDURE AND PATIENT OUTCOME WERE UNKNOWN. NO ADDITIONAL INFORMATION WAS PROVIDED. THIS REPORT IS FOR ONE (1) PEDIATRIC LCP HIP PL 5.0/130/9 HOLES THIS COMPLAINT INVOLVES ONE(1) DEVICE.
Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available
MAUDE report 14252903 ↗
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- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-PLF40Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-PRT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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