Catalog Number UNK KNEE FEMORAL |
Device Problem
Adverse Event Without Identified Device or Use Problem (2993)
|
Patient Problems
Rupture (2208); Not Applicable (3189)
|
Event Date 03/06/2018 |
Event Type
Injury
|
Manufacturer Narrative
|
(b)(4).If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
|
|
Event Description
|
Der states quad repair.Insert was changed.Doi: unknown; dor: (b)(6) 2018 left knee.
|
|
Manufacturer Narrative
|
(b)(4).Investigation summary no device associated with this report was received for examination.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
|
|
Search Alerts/Recalls
|