Acumatch A Series 120-01-62Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885862019783), received between Feb 26, 2020 and Feb 26, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Migration” (1 report).

2 other recalls cover devices cleared under the same FDA submission (K993082); they may or may not involve this specific model.

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.

• InjuryFeb 26, 2020Migration; Migration

  AS REPORTED, THIS MALE PATIENT WAS INITIAL IMPLANTED WITH EXACTECH DEVICES ON AN UNKNOWN DATE, UNKNOWN FACILITY AND UNKNOWN SURGEON. A REVISION SURGERY PERFORMED ON (B)(6) 2001. NO OTHER INFORMATION AVAILABLE ON THE REVISION EXCEPT THAT EXACTECH DEVICES WERE IMPLANTED. THE CURRENT EVENT FOR THIS (B)(6) Y/O MALE PATIENT IS THE ACETABULAR SHELL NEEDED REVISION DUE TO MIGRATING INTO A VERTICAL POSITION. THE CUP/LINER AND TWO SCREWS WERE REMOVED. ACETABULUM WAS REAMED AND COMPETITOR DEVICES WAS IMPLANTED ALONG WITH EXACTECH COCR HEAD 28+5. THE HIP WAS FOUND TO BE STABLE AND WOUND WAS CLOSED. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. DEVICES WILL NOT BE RETURNED DUE TO HOSPITAL POLICY. PHOTO OF EXPLANTED DEVICE WAS PROVIDED.

  Patient problems: Failure of Implant

  MAUDE report 9758232 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K993082. One submission often covers many models, so check the product and lot details in each record.

• Z-1734-2022 · Aug 11, 2022 · Open, Classified
  GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. ACUMATCH 0 DEGREE LINER 28MM 46MM, REF 130-28-05; b. ACUMATCH 0 DEGREE LINER 28MM 48MM, REF 13
• Z-1031-2017 · Nov 7, 2016 · Terminated
  AcuMatch A-Series Connexion GXL Enhanced Polyethylene Acetabular Liner, 15, +5 mm Lateralized, 36 mm I.D., Size J.