Catalog Number 999800102 |
Device Problem
Insufficient Information (3190)
|
Patient Problem
Failure of Implant (1924)
|
Event Date 11/14/2017 |
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.No 510(k) number provided because this implant is sold internationally with different indications for use; it is currently sold in the us under a different part number.
|
|
Event Description
|
Translated claim letter received.Claim letter alleges the patient is experiencing worsening clinical conditions due to a defective depuy prosthetic joint.Doi: (b)(6) 2008; dor: not reported (unknown hip).
|
|
Manufacturer Narrative
|
Product complaint # = > pc-(b)(4).Investigation summary = > the asr platform was voluntarily recalled from the market in august 2010, and the asr product codes are now considered inactive.Further investigation of this individual incident will not be undertaken.The investigation regarding the root cause(s) and/or corrective actions was conducted under mdd capa-(b)(4).Ongoing post market surveillance is conducted per our procedures for this product.If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
|
|
Search Alerts/Recalls
|