LCP 238.707Recalls & reported problems
Synthes (U.S.A.) LP · 3.5MM LCP® MEDIAL DISTAL TIBIA PLATE W/O TAB 10 HOLES-LEFT · Class 2 · Implant
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 10886982162175), received between Jan 3, 2018 and Jan 3, 2018 — 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
- 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.
InjuryJan 3, 2018Break; Break
IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED ON (B)(6) 2017. THE PATIENT WAS IMPLANTED WITH A 3.5MM LOCKING COMPRESSION PLATE (LCP) MEDIAL DISTAL TIBIA PLATE APPROXIMATELY TWO MONTHS PRIOR TO REMOVAL AND, PER THE SURGEON, WAS NON-COMPLIANT AND THE PLATE BROKE. THE PATIENT WAS REVISED TO A SIMILAR PLATE. SURGERY COMPLETED SUCCESSFULLY WITH NO DELAY. CONCOMITANT DEVICES REPORTED: SCREWS (PART NUMBER UNKNOWN, LOT NUMBER UNKNOWN, QUANTITY UNKNOWN). THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: Failure of Implant
MAUDE report 7161610 ↗
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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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