DLP® 94535Recalls & reported problems
Medtronic, Inc. · CANNULA 94535 RCSP PVC AUTO 15FR 10P 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 20613994575832), received between Jun 9, 2025 and Jun 9, 2025 — classified as 1 malfunction.
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
- 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.
MalfunctionJun 9, 2025Break; Break
IT WAS REPORTED THAT DURING AN AORTIC VALVE REPLACEMENT AND BYPASS SURGERY, A SPONTANEOUS BREAK OCCURRED AT THE JUNCTION BETWEEN THE CARDIOPLEGIA CIRCUIT LINE AND THE DLP PVC RCSP CANNULA WITH AUTO-INFLATE CUFF. THE USE OF THE DEVICE WAS UNSPECIFIED. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22165583 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.