MAUDE Adverse Event Report: QUICKLINK¿ CARTRIDGE 5.0MM EXTENSION SOURCELINK¿; BRACHYTHERAPY LINKS & CARTRIDGES

Model Number	70303QC20
Medical Device Problem Codes	Fitting Problem (2183); Physical Resistance/Sticking (4012)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/22/2021
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
As the lot number for the device was provided, a review of the device history record is currently being performed.The device has been returned to the manufacturer for evaluation as well as photo was provided for review.The investigation of the reported event is currently underway.(expiry date: 11/2021).
Event or Problem Description
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 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.
Additional Manufacturer Narrative
H10: manufacturing review: a complaint history review was performed.This is the first complaint reported for this product/lot number combination.However, the device history records were reviewed and there was nothing found to indicate there was a manufacturing related cause for these reports.Investigation summary: one cartridge was returned for evaluation.This sample was used for training in a non-clinical setting, there were 12 links left in the cartridge.The cartridge was inspected and nothing unusual was noted.The cartridge gate closure worked as expected, no spring protrusion on the backside of the cartridge and the plunger traveled appropriately.The cartridge was then placed into a quicklink loader and was able to dispense the links.An attempt was made to link these parts to non-radioactive brachyseeds, which was successful.Additionally, all of the strands passed through the needle adaptor.One photo of strands of links and seeds was received and it was noticed that the links were damaged.The strands were incorrectly built consisting of either 2 female ends placed adjacent to each other, or a female end placed at the beginning or the end of the strand.The investigation is not confirmed for the reported issue.The definitive root cause could not be determined based upon available information.Labeling review: the information for use was reviewed for quicklink delivery system.There is a troubleshooting section described conditions when the sourcelink connectors are not connected to seeds after compression.H10: d4 (expiry date: 11/2021).H11:section a through f - the information provided by bd represents all of the known information at this time.Despite good faith efforts to obtain additional information, the complainant / reporter was unable or unwilling to provide any further patient, product, or procedural details to bd.H3 other text : see h10.
Event or Problem Description
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 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.

• Brand Name: QUICKLINK¿ CARTRIDGE 5.0MM EXTENSION SOURCELINK¿
• Common Device Name: BRACHYTHERAPY LINKS & CARTRIDGES
• MDR Report Key: 12334890
• Report Number: 1018233-2021-05010
• Device Sequence Number: 4542683
• Product Code: KXK
• UDI-Device Identifier: 10801741078115
• UDI-Public: (01)10801741078115
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• PMA/510(K) Number: K023210
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,foreig
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial,Followup
• Report Date (Section B): 09/09/2021

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 70303QC20
• Device Catalogue Number: 70303QC20
• Device Lot Number: BBFR0057
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/16/2021
• Initial Date Received by Manufacturer: 07/22/2021
• Supplement Date Received by Manufacturer: 09/10/2021
• Initial Report FDA Received Date: 08/18/2021
• Supplement Report FDA Received Date: 09/14/2021
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/18/2021
• Is the Device Labeled for Single Use? (Y/N): Yes
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Initial
• Patient Sequence Number: 1