MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-12-17 for PARK BLADE SEPTOSTOMY CATHETER PBS-200 manufactured by Cook Inc.
[131142316]
This mdr is being filed after the associated complaint was reviewed under remediation protocol (b)(4), complaint/mdr retrospective review and remediation and reassessed as reportable. Additional complaint investigation and record remediation was not performed.
Patient Sequence No: 1, Text Type: N, H10
[131142317]
It was reported that the blade of the park blade septostomy catheter was not coming out correctly. Another device was used to finish the procedure. There were no injuries or additional procedures reported.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1820334-2018-03840 |
| MDR Report Key | 8172096 |
| Date Received | 2018-12-17 |
| Date of Report | 2018-12-17 |
| Date of Event | 2015-07-27 |
| Date Mfgr Received | 2018-12-13 |
| Device Manufacturer Date | 2012-07-01 |
| Date Added to Maude | 2018-12-17 |
| 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 | MR. LARRY POOL |
| Manufacturer Street | 750 DANIELS WAY |
| Manufacturer City | BLOOMINGTON IN 47404 |
| Manufacturer Country | US |
| Manufacturer Postal | 47404 |
| Manufacturer Phone | 8128294891 |
| Manufacturer G1 | COOK INC |
| Manufacturer Street | 750 DANIELS WAY |
| Manufacturer City | BLOOMINGTON IN 47404 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 47404 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | PARK BLADE SEPTOSTOMY CATHETER |
| Generic Name | DXF CATHETER, SEPTOSTOMY |
| Product Code | DXF |
| Date Received | 2018-12-17 |
| Model Number | NA |
| Catalog Number | PBS-200 |
| Lot Number | 3507528 |
| Device Expiration Date | 2015-07-01 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COOK INC |
| Manufacturer Address | 750 DANIELS WAY BLOOMINGTON IN 47404 US 47404 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2018-12-17 |