MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06,07 report with the FDA on 2014-08-04 for NEURAGEN NERVE GJIDE 5MM ID X 3CM LENGTH manufactured by Integra Lifesciences Corp..
[4878555]
It was reported "case was performed using expired (neuragen) product". There was no adverse consequence or injury to the patient reported to date.
Patient Sequence No: 1, Text Type: D, B5
[12182789]
The device involved in the reported incident is not available for evaluation. An investigation has been initiated based on the reported information.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1121308-2014-00035 |
MDR Report Key | 4036516 |
Report Source | 06,07 |
Date Received | 2014-08-04 |
Date of Report | 2014-07-17 |
Date of Event | 2014-06-14 |
Date Mfgr Received | 2014-07-17 |
Date Added to Maude | 2014-09-03 |
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 | 0 |
Event Location | 0 |
Manufacturer Contact | CAREN FINKELSTEIN |
Manufacturer Street | 315 ENTERPRISE DRIVE |
Manufacturer City | PLAINSBORO NJ 08536 |
Manufacturer Country | US |
Manufacturer Postal | 08536 |
Manufacturer Phone | 6099362341 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | NEURAGEN NERVE GJIDE 5MM ID X 3CM LENGTH |
Generic Name | NEURAGEN |
Product Code | JXI |
Date Received | 2014-08-04 |
Lot Number | 1122487 |
Device Expiration Date | 2014-05-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | INTEGRA LIFESCIENCES CORP. |
Manufacturer Address | PLAINSBORO NJ 08536 US 08536 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2014-08-04 |