LCP 02.112.094Recalls & reported problems
Synthes GmbH · 3.5MM LCP SUPERIOR CLAVICLE PLATE W/LAT EXTN/8H/RT/130MM · 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 10886982033291), received between Aug 29, 2017 and Aug 29, 2017 — 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.
InjuryAug 29, 2017Break; Break
IT WAS REPORTED THAT A PATIENT UNDERWENT REMOVAL OF A 3.5 MM LCP BROKEN CLAVICLE PLATE W/LAT EXTN/8H/RT/130 MM AND SCREWS ON (B)(6) 2017 DUE TO THE BROKEN PLATE. THE PLATE BROKE IN TWO PIECES. THE PLATE AND SCREWS WERE ORIGINALLY IMPLANTED IN (B)(6) 2017 DURING A REVISION OF A SYNTHES PLATE. ON AN UNKNOWN DATE POSTOPERATIVELY, THE PATIENT WAS PLAYING GOLF WHEN THE PLATE BROKE. THE PLATE AND SCREWS WERE REMOVED AND NOT REPLACED WITH ANY OTHER HARDWARE. THE PATIENT OUTCOME IS UNKNOWN. THIS COMPLAINT INVOLVES ONE PART CONCOMITANT PARTS: SCREWS. THIS REPORT IS 1 OF 1 FOR (B)(4).
Patient problems: Failure of Implant
MAUDE report 6826939 ↗
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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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