FDA Adverse Event Injury Summary report: N

PINNACLE MTL INS NEUT36IDX52OD

MDR report key: 4112863 · Received September 24, 2014

Report

Report Number
1818910-2014-28745
Event Type
Injury
Date Received
September 24, 2014
Date of Event
June 5, 2013
Report Date
August 26, 2014
Manufacturer
DEPUY INTERNATIONAL LTD. 8010379
Product Code
KWA
PMA / PMN Number
PK003523
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

ADDITIONAL NARRATIVE: NO DEVICE ASSOCIATED WITH THIS REPORT WAS RECEIVED FOR EXAMINATION. BASED ON PREVIOUS INVESTIGATIONS THIS COMPLICATION OF JOINT REPLACEMENT IS UNLIKELY TO HAVE BEEN THE RESULT OF A DEVICE FAILING TO MEET REQUIRED SPECIFICATIONS. THE INFORMATION RECEIVED WILL BE RETAINED FOR POTENTIAL SERIES INVESTIGATIONS IF TRIGGERED BY TREND ANALYSIS, POST MARKET SURVEILLANCE, OR OTHER EVENTS WITHIN THE QUALITY SYSTEM. CORRECTIVE ACTION WAS NOT INDICATED. DEPUY CONSIDERS THE INVESTIGATION CLOSED. SHOULD ADDITIONAL INFORMATION BE RECEIVED, THE INFORMATION WILL BE REVIEWED AND THE INVESTIGATION WILL BE RE-OPENED AS NECESSARY.

Additional Manufacturer Narrative · 1

UDI (B)(4). THIS COMPLAINT IS STILL UNDER INVESTIGATION. DEPUY WILL NOTIFY THE FDA OF THE RESULTS OF THIS INVESTIGATION ONCE IT HAS BEEN COMPLETED. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

Description of Event or Problem · 1

REPORT OF FORMAL CLAIM RECEIVED REGARDING PINNACLE/CORAIL HIP REVISION FROM KENNEDYS.REVISION DATE CONFIRMED, REASON FOR REVISION NOT PROVIDED.DOI 2007

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
596168 PINNACLE MTL INS NEUT36IDX52OD HIP ACETABULAR INSERT/LINER KWA DEPUY INTERNATIONAL LTD. 8010379 2381640

Patients

Seq Age Sex Outcome Treatment
1 79 YR Other