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LACTOSORB® SYSTEM 915-1595 (UDI 00888233012027)Recalls & reported problems

Biomet Microfixation, Inc · Class 1

All models of LACTOSORB SYSTEM (7)

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

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

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00888233012027), received between Jan 5, 2021 and Jan 5, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Fracture1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

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

  • MalfunctionJan 5, 2021Fracture; Fracture

    IT WAS REPORTED THE TAP BROKE WHILE THE SURGEON WAS CUTTING THE TAP RESULTING IN A SURGICAL DELAY GREATER THAN THIRTY MINUTES. THE SURGEON DRILLED A HOLE AROUND THE BROKEN TAP WITH A TWIST DRILL AND USED PLIERS TO REMOVE THE TAP. IMAGING REVEALED THERE WAS NO FRAGMENT IN THE PATIENT'S BODY. NO ADDITIONAL PATIENT CONSEQUENCES HAVE BEEN REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions; No Known Impact Or Consequence To Patient

    MAUDE report 11121466 ↗

Other TAP, BONE devices

All TAP, BONE devices →

Sources and updates

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