MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-08-13 for VENTRICLEAR G44130 50318 manufactured by Cook Incorporated.
[116924915]
Patient with a posterior fossa mass status post craniotomy for tumor resection underwent ventriculostomy catheter removal. During the procedure, a 3. 2 cm portion of the distal tip of the external ventricular drain fractured and was retained. The retained segment was then removed in operating room.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 7776931 |
| MDR Report Key | 7776931 |
| Date Received | 2018-08-13 |
| Date of Report | 2018-07-27 |
| Date of Event | 2018-07-13 |
| Report Date | 2018-07-27 |
| Date Reported to FDA | 2018-07-27 |
| Date Reported to Mfgr | 2018-08-13 |
| Date Added to Maude | 2018-08-13 |
| Event Key | 0 |
| Report Source Code | User Facility report |
| Manufacturer Link | N |
| Number of Patients in Event | 0 |
| Adverse Event Flag | 0 |
| 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 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | VENTRICLEAR |
| Generic Name | CATHETER, VENTRICULAR (CONTAINING ANTIBIOTIC OR ANTIMICROBIAL AGENTS) |
| Product Code | NHC |
| Date Received | 2018-08-13 |
| Model Number | G44130 |
| Catalog Number | 50318 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | 3 DA |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | COOK INCORPORATED |
| Manufacturer Address | 750 DANIELS WAY BLOOMINGTON IN 47404 US 47404 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2018-08-13 |