MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,07 report with the FDA on 2014-08-14 for YASARGIL TI PERM STD - CLIP STR 17.5 MM C0068558 manufactured by Aesculap Ag & Co. Kg.
[5035842]
Country of complaint: (b)(6). Complaint states: during an operation, the surgeon confirmed by an image that the clip was fixed an aneurysm properly. Then, after the operation, he confirmed with a ct as well. However, the patient's condition began to deteriorate. The surgeon decided to do a 3d cta. As a result, it was confirmed that the clip had slipped out from the aneurysm. The surgeon reoperated and changed to a sugita clip.
Patient Sequence No: 1, Text Type: D, B5
[12481201]
Us reporting agent notified on: (b)(4) 2014. Manufacturing site evaluation: evaluation is ongoing.
Patient Sequence No: 1, Text Type: N, H10
| Report Number | 2916714-2014-00658 |
| MDR Report Key | 4213833 |
| Report Source | 01,07 |
| Date Received | 2014-08-14 |
| Date of Report | 2014-08-12 |
| Date of Event | 2014-07-13 |
| Date Mfgr Received | 2014-07-14 |
| Device Manufacturer Date | 2013-03-08 |
| Date Added to Maude | 2014-11-06 |
| 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 | 0 |
| Initial Report to FDA | 3 |
| Report to FDA | 0 |
| Event Location | 0 |
| Manufacturer Contact | MICHELLE LINK |
| Manufacturer Street | 615 LAMBERT POINTE DR. |
| Manufacturer City | HAZELWOOD MO 63042 |
| Manufacturer Country | US |
| Manufacturer Postal | 63042 |
| Manufacturer Phone | 3145515938 |
| Manufacturer G1 | AESCULAP AG&CO KG |
| Manufacturer Street | PO BOX 40 |
| Manufacturer City | TUTTLINGEN 78501 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 78501 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | YASARGIL TI PERM STD - CLIP STR 17.5 MM |
| Generic Name | VASCULAR CLIP |
| Product Code | HCH |
| Date Received | 2014-08-14 |
| Model Number | C |
| Catalog Number | C0068558 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | * |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | AESCULAP AG & CO. KG |
| Manufacturer Address | TUTTLINGEN 78532 GM 78532 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Hospitalization; 2. Other; 3. Required No Informationntervention | 2014-08-14 |