MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-12-03 for PUMP MAX CANISTER PAPS2 manufactured by Penumbra, Inc..
[169025549]
This device is available for return. A follow up mdr will be submitted upon completion of the device investigation.
Patient Sequence No: 1, Text Type: N, H10
[169025550]
The patient was undergoing a thrombectomy procedure in the middle cerebral artery (mca) using a penumbra max canister (canister). During the procedure, the physician noticed that the tubing connected to the filter of the penumbra system aspiration pump max 110 (pump max) had blood in it; therefore, the canister was removed. The procedure was completed using another canister and the same pump max. There was no report of an adverse effect to the patient.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3005168196-2019-02230 |
| MDR Report Key | 9407007 |
| Report Source | COMPANY REPRESENTATIVE,HEALTH |
| Date Received | 2019-12-03 |
| Date of Report | 2019-11-07 |
| Date of Event | 2019-11-01 |
| Report Date | 2005-01-01 |
| Date Reported to FDA | 2005-01-01 |
| Date Reported to Mfgr | 2005-01-10 |
| Date Mfgr Received | 2020-02-21 |
| Date Added to Maude | 2019-12-03 |
| Event Key | 0 |
| Report Source Code | Manufacturer report |
| Manufacturer Link | Y |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 3 |
| Product Problem Flag | 3 |
| Reprocessed and Reused Flag | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MS. VERONICA FARRIS |
| Manufacturer Street | ONE PENUMBRA PLACE |
| Manufacturer City | ALAMEDA CA 94502 |
| Manufacturer Country | US |
| Manufacturer Postal | 94502 |
| Manufacturer Phone | 5107483200 |
| Single Use | 0 |
| Previous Use Code | 0 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PUMP MAX CANISTER |
| Generic Name | JCX |
| Product Code | JCX |
| Date Received | 2019-12-03 |
| Returned To Mfg | 2019-11-18 |
| Model Number | PAPS2 |
| Catalog Number | PAPS2 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | R |
| Device Age | DA |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | PENUMBRA, INC. |
| Manufacturer Address | ONE PENUMBRA PLACE ALAMEDA CA 94502 US 94502 |
| Product Code | --- |
| Date Received | 2019-12-03 |
| Device Sequence No | 101 |
| Device Event Key | 0 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-12-03 |