DLP® 10052Recalls & reported problems
Medtronic, Inc. · SUCTION 10052 6FR SHAFT10FR SOFT TIP 17L · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 20613994698319), received between Jun 19, 2018 and Dec 8, 2025 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Device Slipped” (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-1804-2024 · Root cause: Process control · FDA record ↗
Most reported problems
Device problems
- Device Slipped1
- Material Separation1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionDec 8, 2025Material Separation; Material Separation
IT WAS REPORTED THAT DURING CORONARY ARTERY BYPASS GRAFTING SURGERY, THE FINE CORONARY SUCTION TIP OF THE DLP CARDIAC SUCTION TUBE CAME AWAY FROM THE SHAFT. THE CUSTOMER STATED THAT THE BLUE TIP CAME AWAY FROM THE SHAFT WITH SUCH EASE THAT IT COULD EASILY BE LOST IN THE PATIENT¿S CHEST CAVITY. 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 23740292 ↗MalfunctionJun 19, 2018Device Slipped; Device Slipped
MEDTRONIC RECEIVED INFORMATION THAT DURING USE WHILE DOING THE ROUTINE COUNT CHECK, THE SCRUB NURSE DISCOVERED THE SOFT TIP OF THE CANNULA HAD DROPPED OFF. IT WAS FOUND WITHIN THE PATIENT'S CHEST WALL. THE PRODUCT WAS REPLACED. THERE WAS NO ADVERSE EFFECT TO THE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7613155 ↗
Other SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS devices
- DLP® 10050Medtronic, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS1 recall6 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
- DLP® 10051Medtronic, Inc. · SUCKER, CARDIOTOMY RETURN, CARDIOPULMONARY BYPASS2 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 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 · each recall links to the FDA recall notice
- 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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