FDA Adverse Event Injury Summary report: N

DEPUY CMW 2G 20G

MDR report key: 3843409 · Received June 2, 2014

Report

Report Number
1818910-2014-19893
Event Type
Injury
Date Received
June 2, 2014
Date of Event
May 14, 2014
Report Date
January 14, 2016
Manufacturer
DEPUY CMW REG. # 9610921
Product Code
LOD
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
OTHER

Narratives

Additional Manufacturer Narrative · 1

THE INVESTIGATION REMAINS CLOSED, AS THIS CORRECTED INFORMATION DOES NOT HAVE ANY IMPACT ON THE OUTCOME OF THE INVESTIGATION.

Additional Manufacturer Narrative · 1

THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED.

Additional Manufacturer Narrative · 1

THE DEVICE ASSOCIATED WITH THIS REPORT WAS NOT RETURNED. A COMPLAINT DATABASE SEARCH FINDS NO OTHER RELATED INCIDENTS AGAINST THE PROVIDED PRODUCT AND LOT COMBINATION. PER REQUEST BY CUSTOMER, A DHR REVIEW WAS CONDUCTED ON THE PROVIDED PRODUCT/LOT COMBINATION. THE INITIAL REPORTING STATED NO ADDITIONAL INVESTIGATIONAL INPUTS WERE AVAILABLE. THE INVESTIGATION COULD NOT VERIFY OR IDENTIFY ANY PRODUCT CONTRIBUTION TO THE REPORTED EVENT WITH THE INFORMATION PROVIDED. BASED ON THE INABILITY TO IDENTIFY ROOT CAUSE, THE NEED FOR CORRECTIVE ACTION WAS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY.

Description of Event or Problem · 1

PROCEDURE: KNEE REVISION. ORIGINALLY IMPLANTED IN (B)(6) 2012. REVISION SURGERY WAS PERFORMED ON (B)(6) 2014 BY THE SAME SURGEON. REASON FOR REVISION WAS DUE TO ONGOING PAIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
321491 DEPUY CMW 2G 20G CEMENT / CEMENT ACCESSORY LOD DEPUY CMW REG. # 9610921 3444978

Patients

Seq Age Sex Outcome Treatment
1 57 YR Required Intervention