Acumatch A Series 120-01-60Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885862019776), received between Feb 12, 2020 and Feb 12, 2020 — classified as 1 injury.

The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (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 12, 2020Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth

  AS REPORTED, THE ORIGINAL LEFT TOTAL HIP ARTHROPLASTY ON THIS (B)(6) Y/O MALE PATIENT WAS PERFORMED ON (B)(6) 2007. THIS PATIENT WAS REVISED DUE TO THE ACETABULAR SHELL APPEARS TO BE LOOSE. THE SURGEON OPENED THE PATIENT AND DISSECTED DOWN TO THE JOINT SPACE. HE DISLOCATED THE HIP AND REMOVED THE FEMORAL HEAD, THEN PROCEEDED TO REMOVE THE ACETABULAR SHELL, LINER, AND TWO SCREWS. A COMPETITOR SHELL AND LINER WAS PLACED. HE REPLACED THE PREVIOUS FEMORAL HEAD WITH THE SAME SIZE (36MM -3.5 OFFSET). THE SURGEON WAS HAPPY WITH THESE IMPLANTS AND CLOSED THE PATIENT. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. DEVICES WILL NOT BE RETURNED DUE TO HOSPITAL POLICY.

  Patient problems: Failure of Implant

  MAUDE report 9699795 ↗

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.