Acumatch A Series 120-01-50Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10885862019721), received between Jul 18, 2023 and May 22, 2024 — classified as 2 injuries.

The most frequently reported specific device problem is “Loosening of Implant Not Related to Bone-Ingrowth” (2 reports).

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 16, 2026.

Most reported problems

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

• InjuryMay 22, 2024Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth

  IT WAS REPORTED THAT THIS 86 Y/O FEMALE PATIENT'S LEFT HIP WAS REVISED. PATIENT HAD A DISSOCIATED CUP. STEM WAS LEFT IN, ONLY FEMORAL HEAD WAS REVISED TO EXACTECH. ACETABULAR SIDE WAS REVISED TO A COMPETITORS DEVICE. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT . DEVICES ARE NOT RETURNING - HOSPITAL POLICY.

  Patient problems: Failure of Implant

  MAUDE report 19373914 ↗
• InjuryJul 18, 2023Loosening of Implant Not Related to Bone-Ingrowth; Loosening of Implant Not Related to Bone-Ingrowth

  AS REPORTED, APPROXIMATELY 15 YEARS POST OP INITIAL RIGHT THA, THIS 79 Y/O FEMALE PATIENT WAS REVISED DUE TO THE ACETABULAR COMPONENTS BECOMING LOOSE. PATIENT'S FEMORAL HEAD WAS REVISED USING EXACTECH. 170-32-50, BIOLOX DELTA OPTION HEAD, 32MM AND 170-50-03, BIOLOX DELTA ADAPTER, 12/14 +3.5MM, THE ACETABULAR SIDE WERE REVISED TO COMPETITORS DEVICE. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. UNKNOWN MEDICAL HISTORY. NO PICTURES OR X-RAYS PROVIDED. DEVICE NOT BEING RETURNED DUE TO HOSPITAL POLICY.

  Patient problems: Failure of Implant; Metal Related Pathology; Osteolysis

  MAUDE report 17343117 ↗

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.