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QuickLink™, SourceLink™ 70301QC20Recalls & reported problems

Bard Brachytherapy, Inc. · QuickLink™ Cartridge with 5.5mm Standard SourceLink™ Connectors · Class 2 · Implant

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 10801741078078), received between Feb 1, 2022 and Mar 16, 2022 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Physical Resistance/Sticking” (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.

Most reported problems

Device problems

  • Physical Resistance/Sticking2

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.

  • MalfunctionMar 16, 2022Physical Resistance/Sticking; Physical Resistance/Sticking

    IT WAS REPORTED THAT DURING A BRACHYTHERAPY PROCEDURE, THE CONNECTOR WAS ALLEGEDLY STUCK WITHIN THE NEEDLE ADAPTER, AND COULD NOT BE INSERTED INTO THE RELAY APPLICATOR. THE SEEDS AND A CONNECTOR WERE COLLECTED IN THE NEXT DAY. THERE WAS NO REPORTED PATIENT INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13786372 ↗
  • MalfunctionFeb 1, 2022Physical Resistance/Sticking; Physical Resistance/Sticking

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

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 13419891 ↗

Other Source, brachytherapy, radionuclide devices

All Source, brachytherapy, radionuclide devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.