LCP 02.112.108Recalls & reported problems
Synthes GmbH · 2.7MM/3.5MM LCP POSTLAT DISTAL FIBULA PLATE 4H/RIGHT/90MM · Class 2 · Implant
All models of LCP (367)
Data updated Oct 18, 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 10886982033376), received between Jul 18, 2018 and Jul 18, 2018 — classified as 1 injury.
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.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJul 18, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT ON (B)(6) 2018 THE PATIENT UNDERWENT REMOVAL OF THE LOCKING COMPRESSION PLATE (LCP) POSTEROLATERAL DISTAL FIBULA PLATE AND SIX SCREWS ON THE RIGHT ANKLE DUE TO INFECTION. REMOVAL TOOK PLACE 5 MONTHS AFTER IMPLANTATION ON (B)(6) 2018, ONE (1) LCP POSTLAT DISTAL FIBULA PLATE, TWO (2) UNKNOWN 3.5 CORTEX SCREWS, THREE (3) UNKNOWN 2.7 LOCKING SCREWS AND ONE (1) 2.7 CORTEX SCREW WERE REMOVED. THERE WAS NO SURGICAL DELAY REPORTED. PATIENT SURGERY WAS SUCCESSFULLY COMPLETED. THIS REPORT IS FOR (1) 2.7MM/3.5MM LCP POSTLAT DISTAL FIBULA PLATE 4H/RIGHT/90MM. THIS IS REPORT 1 OF 4 FOR COMPLAINT (B)(4).
Patient problems: Unspecified Infection
MAUDE report 7698955 ↗
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- PRECICE® Bone Transport System STP3.5-400Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-225Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-300Nuvasive Specialized Orthopedics, Inc. · Screw, 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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