QuickLink™, SourceLink™ 70302QC10Recalls & reported problems

Summary

The FDA's MAUDE database contains 10 adverse event reports that list this exact device (DI 10801741078092), received between Sep 18, 2017 and Dec 2, 2024 — classified as 10 malfunctions.

The most frequently reported specific device problem is “Sticking” (4 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 10 most recent of 10 reports, in the reporter's own words as published by the FDA.

• MalfunctionDec 2, 2024Material Fragmentation; Mechanical Jam; Material Fragmentation; Mechanical Jam

  IT WAS REPORTED THAT DURING A BRACHYTHERAPY PROCEDURE, THE LINKER CONNECTOR ALLEGEDLY DID NOT EJECT AND GOT STUCK AT THE ENTRANCE OF THE ASSEMBLY BASE. THERE WAS NO REPORTED PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 20816299 ↗
• MalfunctionFeb 1, 2022Physical Resistance/Sticking; Physical Resistance/Sticking

  IT WAS REPORTED THAT DURING A BRACHYTHERAPY PROCEDURE, THE SEEDS ALLEGEDLY COULD NOT BE DISCHARGED FROM THE LOADER. THERE WAS NO REPORTED PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 13415600 ↗
• MalfunctionOct 12, 2021Physical Resistance/Sticking; Physical Resistance/Sticking

  IT WAS REPORTED THAT DURING A BRACHYTHERAPY PROCEDURE, THE CONNECTOR ALLEGEDLY COULD NOT BE DISCHARGED. WHEN THE DISPENSE BUTTON ON THE LOADER WAS PRESSED, THE DISPENSE BUTTON WAS HARD AND THE CONNECTOR COULD NOT BE DISCHARGED, AND THE SEEDS GOT STUCK IN THE LOADER THREE TIMES. THERE WAS NO REPORTED PATIENT INVOLVEMENT.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12614379 ↗
• MalfunctionSep 29, 2021Physical Resistance/Sticking; Physical Resistance/Sticking

  IT WAS REPORTED THAT DURING A BRACHYTHERAPY PROCEDURE, THE CONNECTOR ALLEGEDLY COULD NOT BE DISCHARGED ALTHOUGH THE CONNECTOR WAS SET CORRECTLY ON THE LOADER. THERE WAS NO REPORTED PATIENT INJURY.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 12547689 ↗
• MalfunctionOct 25, 2019Inadequate Instructions for Healthcare Professional; Manufacturing, Packaging or Shipping Problem; Inadequate Instructions for Healthcare Professional

  IT WAS REPORTED THAT THE CUSTOMER ORDERED ITEM 70302QC10, BUT RECEIVED ITEM 70301QC20. THE CUSTOMER WAS ABLE TO COMPLETE THE PROCEDURE WITH THE REQUIRED CONNECTORS, AS THEY STILL HAD SOME ON STOCK.

  Patient problems: No Known Impact Or Consequence To Patient; No Patient Involvement

  MAUDE report 9240469 ↗
• MalfunctionFeb 5, 2018Sticking; Obstruction of Flow

  IT WAS REPORTED THAT THE SEEDS WERE STUCK IN THE NEEDLE WHEN THE RADIOTHERAPIST PUT THEM IN PLACE.

  Patient problems: No Consequences Or Impact To Patient; No Known Impact Or Consequence To Patient

  MAUDE report 7242241 ↗
• MalfunctionFeb 5, 2018Sticking

  IT WAS REPORTED THAT THE SEEDS WERE STUCK IN THE NEEDLE WHEN THE RADIOTHERAPIST PUT THEM IN PLACE.

  Patient problems: No Consequences Or Impact To Patient; No Information

  MAUDE report 7242235 ↗
• MalfunctionFeb 5, 2018Sticking; Obstruction of Flow

  IT WAS REPORTED THAT THE SEEDS WERE STUCK IN THE NEEDLE WHEN THE RADIOTHERAPIST PUT THEM IN PLACE. THE CUSTOMER THOUGHT THE PROBLEM CAME FROM THE SPACER.

  Patient problems: No Consequences Or Impact To Patient; No Information

  MAUDE report 7241244 ↗
• MalfunctionOct 17, 2017Difficult to Remove; Sticking

  IT WAS REPORTED THAT THE CONNECTOR WAS STICKY, SO IT WAS DIFFICULT TO DISCHARGE TO THE ASSEMBLY BASE.

  Patient problems: No Information

  MAUDE report 6954078 ↗
• MalfunctionSep 18, 2017Connection Problem

  IT WAS REPORTED THAT THERE WAS A CONNECTION PROBLEM BETWEEN A CONNECTOR AND A SEED IN THE QUICKLINK LOADER. MEDICON INITIAL VISUAL INSPECTION CONFIRMED THAT THERE WAS NO DEFECT IN APPEARANCE ON THE RETURNED SAMPLE. IT IS UNKNOWN IF ALL THE SEEDS WERE DELIVERED AND/OR IF THERE WAS A PROLONGATION IN PROCEDURE.

  Patient problems: No Known Impact Or Consequence To Patient

  MAUDE report 6873883 ↗