ANTHOLOGY 71357004Recalls & reported problems

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 03596010559470), received between Aug 27, 2018 and May 7, 2021 — classified as 5 injuries.

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

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

• InjuryMay 7, 2021Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  US LEGAL MDL: IT WAS REPORTED THAT A REVISION SURGERY WAS PERFORMED ON (B)(6) 2021 DUE TO A HARDWARE FAILURE THAT OCCURRED ON (B)(6) 2021. THE PATIENT REPORTED THAT SHE WAS WORKING AS A WAITRESS WHEN SHE FELT A POP IN HER RIGHT HIP. RADIOGRAPHS SHOWED FRACTURE OF THE FEMORAL COMPONENT AT THE NECK. STEM, FEMORAL HEAD AND LINER WERE EXTRACTED. PRIMARY SURGERY WAS PERFORMED ON (B)(6) 2019 DUE TO OSTEOARTHRITIS RESULTING FROM RIGHT HIP DYSPLASIA.

  Patient problems: Failure of Implant

  MAUDE report 11794387 ↗
• InjuryApr 7, 2021Break; Break

  IT WAS REPORTED THAT, PATIENT HAD A INITIAL THR SURGERY ON (B)(6) 2019. PATIENT SUFFERED A FRACTURE, THE ANTHOLOGY SO POR PL HA SZ 4 SNAPPED AT THE NECK JUNCTURE THEREFORE IT WAS NECESSARY A REVISION SURGERY. PATIENT OUTCOME IS UNKNOWN.

  Patient problems: Hip Fracture

  MAUDE report 11627544 ↗
• InjuryFeb 5, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  IT WAS REPORTED THAT PATIENT HAD LOW HAEMOGLOBIN AND LOW BLOOD PRESSURE. PATIENT RECEIVED 2 UNITS OF BLOOD TRANSFUSION.

  Patient problems: Injury

  MAUDE report 9671035 ↗
• InjuryJan 22, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

  IT WAS REPORTED THAT THE PATIENT PRESENTS ILIOPSOAS TENDINITIS ON OPERATIVE HIP. THIS WAS FOUND AFTER SURGERY. DEVICE BACK UP NOT APPLICABLE AND DELAY DURING PROCEDURE IS UNKNOWN.

  Patient problems: Injury

  MAUDE report 8266434 ↗
• InjuryAug 27, 2018Device Dislodged or Dislocated

  IT WAS REPORTED A SUBLUXATION OF HEAD OF FEMORAL COMPONENT OF HIP IMPLANT DUE TO LIGAMENTOUS LAXITY. EVENT WAS TREATED WITH REST. NO DELAY TO THE PROCEDURE.SUBJECT ID: (B)(4); AE#4. DATE OF SURGERY: (B)(6) 2017; AGE: (B)(6); SEX: FEMALE.

  Patient problems: Damage to Ligament(s); Joint Dislocation

  MAUDE report 7820493 ↗