LCP 02.120.704Recalls & reported problems
Synthes GmbH · 3.5MM LCP POSTEROMEDIAL PROXIMAL TIBIA PLATE 4H/105MM · 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 10886982040244), received between Jun 25, 2018 and Jun 25, 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
- No Code Available1
- Unspecified Infection1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 25, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE PATIENT UNDERWENT REMOVAL OF ELEVEN (11) LOCKING SCREWS, FOUR (4) CORTEX SCREWS, ONE (1) CANNULATED SCREW, ONE (1) VARIABLE ANGLE LOCKING COMPRESSION (LCP) PROXIMAL TIBIA PLATE, AND ONE (1) LCP POSTEROMEDIAL PROXIMAL TIBIA PLATE DUE TO INFECTION. THERE WAS NO DELAY IN SURGERY. PATIENT OUTCOME WAS NOT REPORTED. THIS REPORT IS FOR ONE (1) 3.5MM LCP POSTEROMEDIAL PROXIMAL TIBIA PLATE 4H/105MM THIS IS REPORT 2 OF 5 FOR (B)(4).
Patient problems: No Code Available; Unspecified Infection
MAUDE report 7634248 ↗
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- PRECICE® Plating System LP4.5-MLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-MRT42Nuvasive 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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