DLP® 69312Recalls & reported problems
Medtronic, Inc. · CANNULA 69312 VEN RT METAL 12FR 10PK 17L · Class 2
Data updated Oct 13, 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 20613994879275), received between Jul 3, 2023 and Jul 3, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Deformation” (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.
Most reported problems
Device problems
- Material Deformation1
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.
MalfunctionJul 3, 2023Material Deformation; Material Deformation
MEDTRONIC RECEIVED INFORMATION THAT DURING USE, THE CUSTOMER REPORTED THE SINGLE STAGE VENOUS CANNULA WAS IN THE SUPERIOR VENA CAVA BUT COULD NOT DRAIN THE BLOOD. THEY REMOVED THE CANNULA AND NOTICED IT WAS DAMAGED. THEY SEARCHED THE SAME LOT AND SAW THE SAME PROBLEM IN ANOTHER CANNULA. THE DEVICE WAS REPLACED. THERE WAS NO ADVERSE EFFECT TO THE PATIENT. THE RETURNED CANNULA WAS THE ONE NOTED TO BE DAMAGED DURING USE. THE SECOND CANNULA WILL NOT BE RETURNED. NO INTERVENTION WAS REQUIRED, THE CANNULA WAS REMOVED AS NORMAL FROM THE PATIENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17246152 ↗
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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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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