MC2® 91229Recalls & reported problems
Medtronic, Inc. · CANNULA 91229 MC2 VEN 29/37FR 10PK 17L · Class 2
- 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 20643169463053), received between May 28, 2025 and May 28, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Contamination” (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
- Contamination1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 28, 2025Contamination; Contamination
IT WAS REPORTED THAT A BLACK HAIR WAS OBSERVED INSIDE THE UNOPENED STERILE PACKAGE OF A MC2 TWO STAGE VENOUS CANNULA. THE FOREIGN MATERIAL (FM) WAS VISIBLE THROUGH THE CLEAR PLASTIC MATERIAL. THE STERILE BARRIER REMAINED SEALED WHEN THE FOREIGN MATERIAL WAS IDENTIFIED. THE DEVICE WAS REPLACED TO COMPLETE THE CASE. THERE WAS NO PATIENT INVOLVED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22094568 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.