MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 03,05 report with the FDA on 2003-11-14 for OCU-GUARD UNK * manufactured by Synovis Surgical Innovations.
        [17832422]
Pt underwent enucleation procedure (date unk) followed by implantation of hydroxyapatite obrital prosthesis implant along with ocu-guard orbital implant wrap. At 1 year post-implant pt presented with chronic pain in eye socket, requiring removal of the device.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 2183620-2003-00040 | 
| MDR Report Key | 495778 | 
| Report Source | 03,05 | 
| Date Received | 2003-11-14 | 
| Date of Report | 2003-10-15 | 
| Date Mfgr Received | 2003-10-15 | 
| Date Added to Maude | 2003-11-19 | 
| 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 | 0 | 
| Manufacturer Contact | PAUL HARTZELL | 
| Manufacturer Street | 2575 UNIVERSITY AVE W | 
| Manufacturer City | ST. PAUL MN 551141024 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 551141024 | 
| Manufacturer Phone | 6516033732 | 
| Manufacturer G1 | SYNOVIS SURGICAL INNOVATIONS | 
| Manufacturer Street | 2575 UNIVERSITY AVE W | 
| Manufacturer City | ST. PAUL MN 55114102 | 
| Manufacturer Country | US | 
| Manufacturer Postal Code | 55114 1024 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | OCU-GUARD | 
| Generic Name | ORBITAL IMPLANT WRAP | 
| Product Code | MTZ | 
| Date Received | 2003-11-14 | 
| Model Number | UNK | 
| Catalog Number | * | 
| Lot Number | UNK | 
| ID Number | * | 
| Operator | HEALTH PROFESSIONAL | 
| Device Availability | N | 
| Device Eval'ed by Mfgr | R | 
| Implant Flag | Y | 
| Date Removed | A | 
| Device Sequence No | 1 | 
| Device Event Key | 484509 | 
| Manufacturer | SYNOVIS SURGICAL INNOVATIONS | 
| Manufacturer Address | 2575 UNIVERSITY AVE. W ST. PAUL MN 551141024 US | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2003-11-14 |