ANTHOLOGY 71357106Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 03596010559616), received between Sep 21, 2017 and Nov 28, 2023 — classified as 5 injuries.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (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 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryNov 28, 2023Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT, DURING THR SURGERY, AFTER AN ANTHOLOGY HO POR PL HA SZ 6 WAS PLACED IN THE PATIENT THE SURGEON REALIZED THAT HE HAD CHOSEN THE WRONG STEM SIZE, FOR WHICH HE DECIDED TO REMOVE IT AND PLACE A NEW SIZE STEM. THE REASON FOR THE WRONG STEM SIZE SELECTION IS UNCERTAIN, AS NO PRODUCT MALFUNCTION HAS BEEN INDICATED. SURGERY WAS COMPLETED WITHOUT DELAY WITHOUT FURTHER ISSUES.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18223393 ↗
• InjuryJan 28, 2020Unintended Movement; Unintended Movement

  IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED SINCE STEM HAD SUBSIDED AND MOVED INTO VARUS AND PATIENT WAS EXPERIENCING THIGH PAIN. WITH THE PATHOLOGY RESULTS AN INFECTION WAS CONFIRMED. AN ANTIBIOTIC SPACER WAS USED.

  Patient problems: Injury; Unspecified Infection

  MAUDE report 9636101 ↗
• InjuryJan 17, 2020Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT REVISION SURGERY WAS PERFORMED DUE TO INFECTION. A FULL SET OF SMITH AND NEPHEW IMPLANTS WERE REIMPLANTED.

  Patient problems: Unspecified Infection

  MAUDE report 9601652 ↗
• InjuryMay 6, 2018Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT HAD FIRST STAGE REVISION HIP ARTHROPLASTY DUE TO INFECTED THR ON (B)(6) 2018 BY DR. (B)(6) AT WOLLONGONG PRIVATE. PRIMARY PROCEDURE WAS DONE AT WOLLONGONG PRIVATE BY DR. STACKPOOL ON (B)(6) 2018.

  Patient problems: Unspecified Infection

  MAUDE report 7489550 ↗
• InjurySep 21, 2017Device Dislodged or Dislocated

  DR REMOVED A SIZE 6 HIGH OFFSET ANTHOLOGY STEM AND REPLACED IT WITH A SIZE 8 HIGH OFFSET STEM DUE TO RECURRENT DISLOCATION.

  Patient problems: Injury; No Code Available

  MAUDE report 6884605 ↗