QuickLink™, SourceLink™ 70303QC10Recalls & reported problems
Bard Brachytherapy, Inc. · QuickLink™ Cartridge with 5.0mm Extension SourceLink™ Connectors · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10801741078108), received between Aug 18, 2021 and Aug 18, 2021 — classified as 1 malfunction.
The most frequently reported specific device problem is “Fitting Problem” (1 report).
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
- Fitting Problem1
- Physical Resistance/Sticking1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 18, 2021Fitting Problem; Physical Resistance/Sticking; Fitting Problem; Physical Resistance/Sticking
IT WAS REPORTED THAT DURING A PROCEDURE, THE DEVICE ALLEGEDLY HAD A CONNECTION PROBLEM WITH THE SEED WHEN EJECTED FROM THE LOADER. IT WAS FURTHER REPORTED THAT INCORRECT RADIATION SOURCE WAS DELIVERED TO THE PATIENT AND BLOCKAGE OF THE SEEDS IN THE NEEDLE WAS NOTED. THERE WAS NO REPORTED PATIENT INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12334902 ↗
Other Source, brachytherapy, radionuclide devices
- QuickLink™, SourceLink™ 70302QC10Bard Brachytherapy, Inc. · Source, brachytherapy, radionuclide10 reports
- QuickLink™, SourceLink™ 70303QC20Bard Brachytherapy, Inc. · Source, brachytherapy, radionuclide7 reports
- QuickLink™, BrachySource™ 1251QCSBard Brachytherapy, Inc. · Source, brachytherapy, radionuclide5 reports
- GammaTile™ GT-001Gt Medical Technologies, Inc. · Source, Brachytherapy, Radionuclide5 reports
- BrachySource™ PS1251LSBard Brachytherapy, Inc. · Source, brachytherapy, radionuclide4 reports
- QuickLink™, BrachySource™ 1251QCLBard Brachytherapy, Inc. · Source, brachytherapy, radionuclide4 reports
- BrachySource™ PS1251CSBard Brachytherapy, Inc. · Source, brachytherapy, radionuclide3 reports
- TheraSeed®, SourceCap™ TS200CSFBard Brachytherapy, Inc. · Source, brachytherapy, radionuclide3 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
- 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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