EVOLUTION® E5001002CNRecalls & reported problems
Microport Orthopedics Inc. · EVOLUTION® 3/8 IN FULLY FLUTED DRILL W/ QUICK DISCONNECT · 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 00192629271548), received between Mar 12, 2024 and Mar 12, 2024 — classified as 1 injury.
The most frequently reported specific device problem is “Break” (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.
Reports received per month
Most reported problems
Device problems
- Break1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryMar 12, 2024Break; Break
ALLEGEDLY, WHEN THE DOCTOR WAS USING THE DRILL FOR THE DISTAL FEMORAL HALL, THE DRILL WAS BLOCKED IN THE FEMORAL CANAL AND WHEN HE PULLED IT OFF, THE TIP OF THE DRILL WASN'T ON THE DRILL ANYMORE, REMAINING IN THE FEMORAL CANAL.
Patient problems: Insufficient Information
MAUDE report 18890917 ↗
Other BIT, SURGICAL devices
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- NA 310.534Synthes GmbH · BIT, SURGICAL64 reports
- NA 4200355042Stryker Corporation · BIT, SURGICAL34 reports
- ACUFEX 72204044Smith & Nephew, Inc. · BIT, SURGICAL25 reports
- NA 03.168.011Synthes GmbH · BIT, SURGICAL20 reports
- ACUFEX 72204042Smith & Nephew, Inc. · BIT, SURGICAL19 reports
- ACUFEX 72204046Smith & Nephew, Inc. · BIT, SURGICAL16 reports
- ACUFEX 72204045Smith & Nephew, Inc. · BIT, SURGICAL14 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.