MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2014-10-03 for LEGION CON ART INS 9MM SZ 5-6 71420537 manufactured by Smith & Nephew, Inc..
[4933622]
It was reported that a revision surgery was performed due to disassociation.
Patient Sequence No: 1, Text Type: D, B5
[12426717]
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1020279-2014-00613 |
MDR Report Key | 4140784 |
Report Source | 07 |
Date Received | 2014-10-03 |
Date of Report | 2014-10-03 |
Date of Event | 2014-10-03 |
Date Facility Aware | 2014-09-26 |
Date Mfgr Received | 2014-09-26 |
Device Manufacturer Date | 2012-02-01 |
Date Added to Maude | 2014-10-03 |
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 | MRS. CONNIE MCBROOM |
Manufacturer Street | 1450 BROOKS ROAD |
Manufacturer City | MEMPHIS TN 38116 |
Manufacturer Country | US |
Manufacturer Postal | 38116 |
Manufacturer Phone | 9013995985 |
Manufacturer G1 | SMITH & NEPHEW, INC. |
Manufacturer Street | 1450 BROOKS ROAD |
Manufacturer City | MEMPHIS TN 38116 |
Manufacturer Country | US |
Manufacturer Postal Code | 38116 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | LEGION CON ART INS 9MM SZ 5-6 |
Generic Name | KNEE IMPLANT |
Product Code | HSA |
Date Received | 2014-10-03 |
Catalog Number | 71420537 |
Lot Number | 12BM78894 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITH & NEPHEW, INC. |
Manufacturer Address | 1450 BROOKS ROAD MEMPHIS TN 38116 US 38116 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2014-10-03 |