Exactech 142-22-00Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885862026729), received between Apr 22, 2020 and Apr 22, 2020 — classified as 1 injury.

1 other recall cover devices cleared under the same FDA submission (K041906); 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. How this data works · Data updated Oct 13, 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.

• InjuryApr 22, 2020Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  AS REPORTED, A (B)(6) Y/O MALE PATIENT, WHO¿S PRIMARY THA WAS IN 1985, PRESENTED WITH HIP DISLOCATIONS DURING HOSPITALIZATION (B)(6) 2019 THAT REQUIRED CLOSED REDUCTIONS. HE COMPLETED ANTIBIOTIC MANAGEMENT WITH NO NEW DISLOCATION EPISODES AND DISCHARGED ON (B)(6) 2019, TO A EXTENDED CARE FACILITY. THE CASE REPORT FORM INDICATES THIS EVENT IS DEFINITELY NOT RELATED TO DEVICES AND POSSIBLE RELATED TO PROCEDURE. THIS EVENT REPORT WAS RECEIVED THROUGH CLINICAL DATA COLLECTION ACTIVITIES. THE CASE REPORT FORM INDICATES THIS EVENT WAS RESOLVED ON (B)(6) 2019 WITH CLOSED REDUCTION. NO DEVICE REMOVED, NONE TO BE RETURNED.

  Patient problems: Bacterial Infection

  MAUDE report 9985855 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K041906. One submission often covers many models, so check the product and lot details in each record.

• Z-1727-2022 · Aug 11, 2022 · Open, Classified
  GXL acetabular liners, orthopedic hip implant component. Product Line Numbers: a. ACUMATCH +5MM LAT LINER 15 DEG 36MM ID, SIZE H, REF 138-36-08 b. ACUMATCH +5MM LAT LINER 15 DE