Anthology AFIT 71935567Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00885556686386), received between Nov 5, 2020 and Nov 5, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Inadequacy of Device Shape and/or Size” (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 18, 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.

• InjuryNov 5, 2020Inadequacy of Device Shape and/or Size; Inadequacy of Device Shape and/or Size

  IT WAS REPORTED THAT, DURING A THA SURGERY, THE IMPLANT SIZE 7 STANDARD OFFSET ANTHOLOGY STEM SAT 5 MM FROM WHERE THE LEVEL OF THE BROACH WAS. THE SURGEON HAD TO EXTRACT AND RE-BROACH SEVEN TIMES. HE ATTEMPTED TO BROACH LARGER WITH THE SIZE 8 BROACH, BUT WAS CONCERNED IF HE ADVANCED IT ANY FURTHER HE WOULD SPLIT THE FEMUR. ULTIMATELY HE COULD NOT SINK THE SIZE 7 IMPLANT TO THE LEVEL HE NEEDED SO HE INSERTED A SIZE 6 WITH A LONGER NECK LENGTH. IT IS UNKNOWN IF THERE WAS A DELAY. THE PATIENT WAS NOT HARMED BEYOND THE DESCRIBED EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions; No Known Impact Or Consequence To Patient

  MAUDE report 10796090 ↗