DLP® 10051Recalls & reported problems
Medtronic, Inc. · SUCTION 10051 6FR SHAFT FRAZIER TIP 17L · Class 2
- 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 20613994698296), received between Apr 11, 2025 and May 2, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Obstruction of Flow” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Obstruction of Flow2
- Suction Problem2
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.
MalfunctionMay 2, 2025Suction Problem; Obstruction of Flow; Suction Problem; Obstruction of Flow
MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF A DLP CARDIAC SUCTION TUBE, IT WAS REPORTED THAT THE SUCTION DID NOT WORK. THE DEVICE WAS REPLACED TO COMPLETE THE PROCEDURE. THERE WAS NO ADVERSE PATIENT EFFECT ASSOCIATED WITH THIS EVENT MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THE PRODUCT DID NOT ASPIRATE THE BLOOD FUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21948484 ↗MalfunctionApr 11, 2025Suction Problem; Obstruction of Flow; Suction Problem; Obstruction of Flow
MEDTRONIC RECEIVED INFORMATION THAT DURING USE OF A DLP CARDIAC SUCTION TUBE, IT WAS REPORTED THAT THE SUCTION DID NOT WORK. THE DEVICE WAS REPLACED TO COMPLETE THE PROCEDURE. THERE WAS NO ADVERSE PATIENT EFFECT ASSOCIATED WITH THIS EVENT. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THE PRODUCT DID NOT ASPIRATE THE BLOOD FUNCTION.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21823627 ↗
Other SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS devices
- DLP® 10050Medtronic, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS1 recall6 reports
- DLP® 10052Medtronic, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS1 recall2 reports
- DLP® 10053Medtronic, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS1 recall2 reports
- DLP® 10060Medtronic, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS1 recall0 reports
- Suction tip SU-xxxxxLivanova USA, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS9 reports
- Suction tip SU-xxxxxLivanova USA, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS6 reports
- Suction tip SU-xxxxxLivanova USA, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS2 reports
- Suction tip SU-xxxxxLivanova USA, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS2 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.