DLP® 10062Recalls & reported problems

Summary

The FDA's MAUDE database contains 7 adverse event reports that list this exact device (DI 20613994570486), received between May 13, 2024 and Sep 1, 2026 — classified as 7 malfunctions.

The most frequently reported specific device problem is “Obstruction of Flow” (7 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.

Most reported problems

Recent adverse event reports

The 7 most recent of 7 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 1, 2026Obstruction of Flow

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50537757 ↗
• MalfunctionMay 30, 2025Obstruction of Flow; Obstruction of Flow

  IT WAS REPORTED THAT PRIOR TO USE OF A DLP RIGID SUCTION TUBE, THERE WERE FLOW ISSUES. THE SUCKER WAS PLUGGED UP AND UNABLE TO APPLY VACUUM. IT WAS NOT CLEAR IF THE SUCKER IS DAMAGED INTERNALLY OR IF THERE IS SOMETHING WITHIN THE BODY THAT IS NOT ALLOWING SUCTION. THERE WAS NO DAMAGE OBSERVED TO THE CANNULA BODY OR TIP. NO ANTICOAGULANT WAS USED. THE ISSUE DID NOT WORSEN OVER TIME. THE DEVICE WAS REPLACED. THERE WAS NO PATIENT INVOLVED IN THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 22112376 ↗
• MalfunctionFeb 18, 2025Obstruction of Flow; Obstruction of Flow

  IT WAS REPORTED THAT THREE DLP RIGID SUCTION TUBES WERE ALLEGEDLY BLOCKED DURING USE. THE DEVICES WERE REPLACED TO COMPLETE THE PROCEDURE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21401214 ↗
• MalfunctionFeb 18, 2025Obstruction of Flow; Obstruction of Flow

  IT WAS REPORTED THAT THREE DLP RIGID SUCTION TUBES WERE ALLEGEDLY BLOCKED DURING USE. THE DEVICES WERE REPLACED TO COMPLETE THE PROCEDURE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21399078 ↗
• MalfunctionFeb 18, 2025Obstruction of Flow; Obstruction of Flow

  IT WAS REPORTED THAT THREE DLP RIGID SUCTION TUBES WERE ALLEGEDLY BLOCKED DURING USE. THE DEVICES WERE REPLACED TO COMPLETE THE PROCEDURE. NO PATIENT COMPLICATIONS HAVE BEEN REPORTED AS A RESULT OF THIS EVENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 21392195 ↗
• MalfunctionSep 20, 2024Obstruction of Flow; Obstruction of Flow

  MEDTRONIC RECEIVED INFORMATION THAT PRIOR TO USE OF A DLP RIGID SUCTION TUBE, IT WAS REPORTED THAT THE DEVICE WAS HOOKED UP PRIOR TO THE START OF THE CASE AND THERE WAS NO SUCTION COMING THROUGH THE DEVICE. THEY TRIED TO RUN STERILE SALINE THROUGH THE DEVICE, HOWEVER, THERE WAS NOTHING COMING THROUGH. THERE WAS NO OBVIOUS DAMAGE OR DEFORMITY OF THE DEVICE. NO PACKAGING ISSUES WERE NOTED UPON DELIVERY. THE USE OF THE DEVICE WAS UNSPECIFIED. THERE WERE NO ADVERSE PATIENT EFFECTS.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20265075 ↗
• MalfunctionMay 13, 2024Contamination; Obstruction of Flow; Contamination; Obstruction of Flow

  MEDTRONIC RECEIVED INFORMATION THAT PRIOR TO USE OF A DLP RIGID SUCTION TUBE, IT WAS REPORTED THAT THE DEVICE WAS CLOGGED. THE DEVICE WAS REPLACED. THERE WAS NO PATIENT INVOLVEMENT, SO NO ADVERSE EFFECT OCCURRED. MEDTRONIC RECEIVED ADDITIONAL INFORMATION THAT THE LUMEN OF TUBE IS OBSTRUCTED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 19296526 ↗