DLP® 69320Recalls & reported problems
Medtronic, Inc. · CANNULA 69320 VEN RT METAL 20FR 10PK 17L · Class 2
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 20613994879237), received between May 1, 2025 and May 1, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Obstruction of Flow” (1 report).
1 FDA recall record name this device's identifier, 1 still open.
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
Recalls naming this device
- Mar 19, 2024Open, Classified
Potential for unsealed sterile packing.
Z-1805-2024 · Root cause: Process control · FDA record ↗
Most reported problems
Device problems
- Obstruction of Flow1
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 1, 2025Obstruction of Flow; Obstruction of Flow
MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF A DLP SINGLE STAGE VENOUS CANNULA WITH RIGHT ANGLE METAL TIP, IT WAS REPORTED THAT CLOT WAS FOUND IN VENOUS CANNULA BY SURGEON UPON REMOVAL FROM THE SVC [SUPERIOR VENA CAVA] AND IVC [INFERIOR VENA CAVA]. DURING THE CASE ACTS [ACTIVATED CLOTTING TIMES] RANGED FROM 460-630 REQUIRING HEPARIN BOLUS ON BYPASS. IT WAS NOTED THAT PERIODICALLY DURING THE CASE THE HEART WOULD FILL UP POSSIBLY INDICATING A DRAINAGE ISSUE. THE CIRCUIT DID HAVE KVAD [KINETIC-ASSISTED VENOUS DRAINAGE] AND TOWARDS THE END OF THE CASE THE KVAD PRESSURES WERE TRENDING UP TO MAINTAIN APPROPRIATE EMPTYING. THE USE OF THE DEVICE WAS NOT SPECIFIED. THERE WAS NO ADVERSE PATIENT EFFECT ASSOCIATED WITH THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21940954 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.