FDA Adverse Event Injury Summary report: N

TAPER SLEEVE ADAPTER 12/14 +2

MDR report key: 2113207 · Received May 20, 2011

Report

Report Number
1818910-2011-08626
Event Type
Injury
Date Received
May 20, 2011
Date of Event
August 9, 2011
Report Date
July 29, 2014
Manufacturer
DEPUY INTERNATIONAL LTD. 8010379
Product Code
KWA
PMA / PMN Number
NA
Removal / Correction Number
Z-1749/1816-2011
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
PATIENT

Narratives

Additional Manufacturer Narrative · 1

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, AS THERE IS AN ONGOING INVESTIGATION REGARDING THE ROOT CAUSE(S) AND/OR CORRECTIVE ACTIONS. (B)(4).

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

IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE. DEPUY STILL CONSIDERS THIS CASE CLOSED TO CAPA.

Description of Event or Problem · 1

THE PT HAS BEEN SCHEDULED FOR AN ASR REVISION. THE SPECIFIC DETAILS REGARDING THE REPORT ARE UNK.

Description of Event or Problem · 1

NEW ETQ RECORD CREATED IN ORDER TO UPDATE ETQ (LEGACY SYSTEM) COMPLAINT NUMBER (B)(4). REASON FOR ORIGINAL COMPLAINT: ASR REVISION. **UPDATE** 1 AUG 2014 - UPDATED DOR FROM CLAIMSUITE DATED 29 JULY 2014. REASON(S) FOR REVISION: PAIN.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 TAPER SLEEVE ADAPTER 12/14 +2 HIP OTHER IMPLANT KWA DEPUY INTERNATIONAL LTD. 8010379 NA 2543041

Patients

Seq Age Sex Outcome Treatment
1 NA Required Intervention