DLP® 94745Recalls & reported problems
Medtronic, Inc. · CANNULA 94745 RCSP SIL AUTO 15FR 10PK · Class 2
All models of DLP (151)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20643169454761), received between Nov 27, 2025 and Nov 27, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (2 reports).
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.
Reports received per month
Most reported problems
Device problems
- Material Deformation2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 27, 2025Material Deformation; Material Deformation
IT WAS REPORTED THAT THESE DLP SILICONE RCSP CANNULAE WITH AUTO-INFLATE CUFFS HAD DAMAGED (PUNCTURED) CUFFS, WHICH MADE IT IMPOSSIBLE TO INFLATE AND PREVENTED THE DEVICES FROM FUNCTIONING PROPERLY PRIOR TO USE. THE DEVICES WERE NOT USED NOR REPLACED. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23664554 ↗MalfunctionNov 27, 2025Material Deformation; Material Deformation
IT WAS REPORTED THAT THESE DLP SILICONE RCSP CANNULAE WITH AUTO-INFLATE CUFFS HAD DAMAGED (PUNCTURED) CUFFS, WHICH MADE IT IMPOSSIBLE TO INFLATE AND PREVENTED THE DEVICES FROM FUNCTIONING PROPERLY PRIOR TO USE. THE DEVICES WERE NOT USED NOR REPLACED. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23664541 ↗
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- EOPA™ 77622Medtronic, Inc. · Catheter, cannula and tubing, vascular, cardiopulmonary bypass2 recalls4 reports
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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