MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-12-18 for PARK BLADE SEPTOSTOMY CATHETER PBS-300 manufactured by Cook Inc.
[130991720]
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
[130991721]
It was reported that prior to patient contact, the blade of the park blade septostomy catheter would not open. It is unknown if/how the procedure was completed, but there were no injuries or additional procedures reported.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1820334-2018-03841 |
MDR Report Key | 8173916 |
Date Received | 2018-12-18 |
Date of Report | 2018-12-18 |
Date of Event | 2015-11-23 |
Date Mfgr Received | 2018-12-13 |
Device Manufacturer Date | 2012-08-01 |
Date Added to Maude | 2018-12-18 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
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 | 2018-12-18 |
Returned To Mfg | 2016-03-15 |
Model Number | NA |
Catalog Number | PBS-300 |
Lot Number | F3647614 |
Device Expiration Date | 2015-08-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
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 | 2018-12-18 |