MULTILOC 04.018.255SRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10886982089472), received between Dec 17, 2021 and Dec 17, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Migration” (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 17, 2021Migration; Migration

  IT WAS REPORTED THAT ON AN UNKNOWN DATE, THE PATIENT UNDERWENT REMOVAL OF MULTILOC HUMERAL NAIL DUE TO ROTATIONAL INSTABILITY THE SURGEON REPORTED THAT THE SURGEON WHO DID THE ORIGINAL SURGERY DID NOT IMPLANT A DISTAL INTERLOCKING SCREW IN THE NAIL. IT WAS ORIGINALLY TREATED IN MID (B)(6) 2021. THE SURGEON SUCCESSFULLY EXPLANTED THE MULTILOC HUMERAL NAIL ON (B)(6) 2021. THE PATIENT OUTCOME WAS UNKNOWN. THIS REPORT INVOLVES ONE (1) 8.5MM TI MULTILOC HUMERAL NAIL RIGHT/CANN/255MM-STERILE. THIS IS REPORT 1 OF 3 FOR (B)(4).

  Patient problems: Appropriate Clinical Signs, Symptoms and Conditions Term/Code Not Available

  MAUDE report 13024839 ↗