LCP 02.112.148Recalls & reported problems
Synthes GmbH · 2.7MM/3.5MM LCP LATERAL DISTAL FIBULA PLATE 9H/RIGHT/151MM · 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 10886982034090), received between Oct 16, 2018 and Oct 16, 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 16, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
Patient problems
- No Code Available1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryOct 16, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED THAT A PATIENT UNDERWENT INITIAL SURGERY ON (B)(6) 2018 TO TREAT AN ANKLE FRACTURE. X-RAY TAKEN ON AN UNKNOWN POSTOPERATIVE DATE REVEALED MALREDUCTION. THE INITIAL PLATE PLACEMENT PUT THE FIBULA IN VALGUS. PATIENT UNDERWENT REVISION SURGERY ON (B)(6) 2018 FOR A HARDWARE REMOVAL. THE PLATE WAS REMOVED, AND A 1/3 TUBULAR WAS USED FOR FINAL FIXATION. THE PROCEDURE WAS COMPLETED SUCCESSFULLY. IT IS UNKNOWN IF THERE WAS A SURGICAL DELAY. PATIENT OUTCOME IS UNKNOWN. THIS REPORT IS FOR ONE (1) 2.7MM/3.5MM LCP LATERAL DISTAL FIBULA PLATE. THIS IS REPORT 1 OF 5 FOR COMPLAINT (B)(4).
Patient problems: No Code Available
MAUDE report 7969034 ↗
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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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