MAUDE Adverse Event Report: PENUMBRA, INC. ARTEMIS NEURO EVACUATION DEVICE; GWG

Catalog Number	AP28
Medical Device Problem Code	Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Code	Hemorrhage, Subdural (1894)
Date of Event	01/30/2019
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
The product was not returned for evaluation.From the information provided, there is no indication that there was any device malfunction, nonconformance, or misuse that contributed to the reported event.Potential adverse events in the labeling with the artemis neuro evacuation device include, but are not limited to, re-bleeding, intraventricular hemorrhage, thromboembolic events, including death.Therefore, it was determined that the reported adverse events were anticipated complications.The manufacturing records for this lot were reviewed and did not reveal any outstanding discrepancies, design, or quality concerns.
Event or Problem Description
On (b)(6) 2019, the patient underwent a minimally invasive surgery (mis) using an artemis neuro evacuation device (artemis).It was reported that the ct scan showed the patient had a re-bleeding intracerebral hemorrhage (ich).Therefore, the patient underwent another mis with an artemis.The patient was discharged to a rehabilitation center on (b)(6) 2019.This re-bleeding ich was adjudicated to be an adverse event related to the artemis, the index ich, the index procedure, and to the comorbidity with the atrial fibrillation which required treatment with eliquis.
Additional Manufacturer Narrative
Please note that the following sections are being updated based on additional information provided by a penumbra sales representative on 06/06/2019.
Event or Problem Description
On (b)(6) 2019, the patient underwent a minimally invasive surgery (mis) using an artemis neuro evacuation device (artemis).It was reported that the ct scan showed the patient had a re-bleeding intracerebral hemorrhage (ich).Therefore, the patient underwent another mis with an artemis.The patient was discharged to a rehabilitation center on (b)(6) 2019.This re-bleeding ich was adjudicated to be a serious adverse event related to the artemis, the index ich, the index procedure, and to the comorbidity with the atrial fibrillation which required treatment with eliquis.

• Brand Name: ARTEMIS NEURO EVACUATION DEVICE
• Common Device Name: GWG
• Manufacturer (Section D): PENUMBRA, INC.; one penumbra place; alameda CA 94502
• MDR Report Key: 8660813
• Report Number: 3005168196-2019-01078
• Device Sequence Number: 11374052
• Product Code: GWG
• UDI-Device Identifier: 00814548017877
• UDI-Public: 00814548017877
• Combination Product (Y/N): Y
• Initial Reporter State: NY
• Initial Reporter Country: US
• PMA/510(K) Number: K171332
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative,health
• Initial Reporter Occupation: Physician
• Type of Report: Initial,Followup
• Report Date (Section B): 05/03/2019
• Report Date (Section F): 01/01/2005

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Expiration Date: 01/22/2021
• Device Catalogue Number: AP28
• Device Lot Number: S10005
• Was Device Available for Evaluation?: No
• Was the Report Sent to FDA?: Yes
• Date Report to Manufacturer: 01/10/2005
• Initial Date Received by Manufacturer: 05/03/2019
• Supplement Date Received by Manufacturer: 06/06/2019
• Initial Report FDA Received Date: 05/31/2019
• Supplement Report FDA Received Date: 06/28/2019
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Age: 73 YR
• Date Report Sent to FDA: 01/01/2005