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Exactech 142-32-07Recalls & reported problems

Exactech, Inc. · Class 2 · Implant

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10885862026859), received between Mar 11, 2022 and Mar 11, 2022 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1

Patient problems

  • Osteolysis1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • InjuryMar 11, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

    AS REPORTED, APPROXIMATELY 3.5 YEARS POST INITIAL THA, THIS MALE PATIENT WAS BROUGHT BACK FOR RIGHT HIP OSTEOLYSIS. THE PATIENT WAS COMPLAINING OF PAIN, AND IT WAS EVIDENT IN THE X RAYS. THE FEMUR WAS DISLOCATED. THE FEMORAL HEAD REMOVED. THE POLY LINER REMOVED USING A BONE SCREW. THE ACETABULAR SCREW WAS REMOVED. THE CUP WAS FOUND TO BE WELL FIXED. A NEW XLE LINER WAS IMPLANTED, 36MM ID LIPPED. THE STEM WAS CHECKED FOUND TO BE LOOSE. IT WAS REMOVED AND A 19X245 MONOBLOC WAS IMPLANTED WITH A 36+3.5 BIOLOX HEAD. THERE WAS NO BREAKAGE OF DEVICE AND NO SURGICAL DELAY/PROLONGATION. PATIENT WAS LAST KNOWN TO BE IN STABLE CONDITION FOLLOWING THE EVENT. X-RAYS ATTACHED. THE DEVICES WILL BE RETURN.

    Patient problems: Osteolysis

    MAUDE report 13732970 ↗

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

Other Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented devices

All Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented devices →

Sources and updates

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