Acumatch A Series 132-32-07Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10885862023209), received between Oct 10, 2019 and Apr 13, 2023 — classified as 2 injuries.

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

1 FDA recall record name this device's identifier, 1 still open.

1 other recall 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.

Recalls naming this device

1. Aug 11, 2022Class IIOpen, Classified

   Specific GXL acetabular polyethylene liners, packaged in non-conforming bags, may adversely impact the device and contribute to accelerated wear.

   Z-1734-2022 · Root cause: Process control · Recall details · FDA record ↗

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.

• InjuryApr 13, 2023Naturally Worn; Naturally Worn

  AS REPORTED, APPROXIMATELY EIGHTEEN YEARS POST INITIAL LEFT THA, THE 82 Y/O FEMALE PATIENT HAD A REVISION DUE TO THE LINER WAS WORN AWAY OVER TIME. THE EXACTECH FEMORAL HEAD WAS SWAPPED FOR A 32MM COCR LONG NECK +5, 11/13 TAPER. SURGEON REMOVED THE EXACTECH LINER AND CEMENTED IN A COMPETITOR'S LINER. THERE WAS NO BREAKAGE OF THE DEVICE OR SURGICAL DELAY/PROLONGATION. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. IMAGES RECEIVED. THE DEVICE IS NOT AVAILABLE FOR EVALUATION DUE TO HOSPITAL POLICY.

  Patient problems: Failure of Implant

  MAUDE report 16737529 ↗
• InjuryOct 10, 2019Unstable

  ORIGINAL RIGHT TOTAL HIP ARTHROPLASTY ON THIS FEMALE PATIENT WAS PERFORMED ON (B)(6) 2004. PATIENT WAS SHOWING MINOR INSTABILITY IN THE HIP TO THE SURGEON PLANNED TO REVISE THE HIP AND UPSIZE THE FEMORAL HEAD AND CHANGE OUT HE LINER. THE SURGEON OPENED THE JOINT IN STANDARD FASHION. THE SURGEON REMOVED THE FEMORAL HEAD IMPLANT. THE SURGEON THEN REMOVED THE ACETABULAR LINER IMPLANT. THE SURGEON TRIALED THE SIZES THEN IMPLANTED THE FINAL IMPLANTS AND CLOSED THE HIP IN STANDARD FASHION. THE PATIENT LEFT THE OPERATING ROOM IN STABLE CONDITION AND IS EXPECTED TO HAVE A GOOD OUTCOME. HOSPITAL DID NOT RELEASE IMPLANTS TO BE RETURNED TO EXACTECH.

  Patient problems: No Code Available

  MAUDE report 9174876 ↗

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-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.