DHHS 282.670SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982179319), received between Dec 28, 2020 and Dec 28, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Device-Device Incompatibility” (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

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryDec 28, 2020Device-Device Incompatibility; Device-Device Incompatibility

  IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE BARREL PLATE WOULDN¿T SEAT OVER BLADE AND BOTH IMPACTOR CAP TIP BROKE IN THE PROCESS. I¿M NOT SURE WHICH ONE WAS AT FAULT SO I WILL GIVE YOU THE NUMBERS FOR THEM ALL. NOTHING WAS LEFT IN THE PATIENT. ENDED UP REMOVING EVERYTHING AND USING CANNULATED SCREWS. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH AN UNKNOWN NUMBER OF SURGICAL DELAYS. THE PATIENT OUTCOME IS UNKNOWN. THIS COMPLAINT INVOLVES FIVE (5) DEVICES. THIS REPORT IS FOR (1) 130 DEG LCP® DHHS(TM) SIDEPLATE-SHRT BARREL 2H-STER. THIS REPORT IS 1 OF 5 FOR (B)(4).

  Patient problems: Failure of Implant

  MAUDE report 11079856 ↗