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ACETABULAR SPTHRM57Recalls & reported problems

Microport Orthopedics Inc. · Class 1

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 M684SPTHRM571), received between Aug 16, 2019 and Aug 16, 2019 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

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

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • No Information1

Recent adverse event reports

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

  • InjuryAug 16, 2019Insufficient Device Problem Information; Insufficient Device Problem Information

    ALLEGEDLY THERE IS OXIDATION/RUSTY ON THE REAMER SURFACE, ESPECIALLY CLOSE TO THE LASER MARKING. SURGERY WAS EXTENDED GREATER THAN 30 MINUTES. KIT NUMBER: SPRMKIT1. KIT LOT NUMBER: G161553.

    Patient problems: No Information

    MAUDE report 8903129 ↗

Other INSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT devices

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.