MAUDE Adverse Event Report: PENUMBRA, INC. RUBY COIL; HCG, KRD

Catalog Number	RBY2C0725
Medical Device Problem Codes	Detachment Of Device Component (1104); Physical Resistance (2578)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	04/17/2017
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The product was not returned for evaluation.Without the return of the device, the root cause of the problem cannot be determined.The manufacturing records for this lot were reviewed and did not reveal any outstanding discrepancies, design, or quality concerns.The device is implanted in the patient.
Event or Problem Description
The patient was undergoing a coil embolization in the splenic artery using ruby coils.During the procedure, while attempting to advance a ruby coil through a px slim delivery microcatheter (px slim), the physician experienced resistance and subsequently, the ruby coil became stuck after being advanced 2/3 into the aneurysm.Therefore, the physician decided to remove it.However, upon retraction, the ruby coil unintentionally detached from the pusher assembly in the patient¿s body and the physician used a snare device to successfully remove the entire detached coil from the patient.While attempting to advance a new ruby coil through the same px slim, the physician experienced resistance and decided to retract the ruby coil.However, upon retraction, the ruby coil unintentionally detached from the pusher assembly within the px slim.The physician was able to securely push the detached coil into the aneurysm and the procedure ended at this point.There was no report of an adverse effect to the patient.

• Brand Name: RUBY COIL
• Common Device Name: HCG, KRD
• Manufacturer (Section D): PENUMBRA, INC.; one penumbra place; alameda CA 94502
• MDR Report Key: 6599527
• Report Number: 3005168196-2017-00820
• Device Sequence Number: 802850
• Product Code: HCG
• UDI-Device Identifier: 00814548012957
• UDI-Public: 00814548012957
• Combination Product (Y/N): N
• Initial Reporter State: AZ
• Initial Reporter Country: US
• PMA/510(K) Number: K120330
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Device Implanted Year: 2017
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Other Health Care Professional
• Type of Report: Initial
• Report Date (Section B): 05/01/2017

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: Physician
• Device Expiration Date: 07/08/2023
• Device Catalogue Number: RBY2C0725
• Device Lot Number: F64826
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/01/2017
• Initial Report FDA Received Date: 05/30/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Patient Age: 24 YR
• Patient Weight: 75