FDA Adverse Event Injury Summary report: N

TOTAL ASR ACET IMP SIZE 50

MDR report key: 3093622 · Received May 6, 2013

Report

Report Number
1818910-2013-05530
Event Type
Injury
Date Received
May 6, 2013
Date of Event
March 29, 2011
Report Date
March 17, 2015
Manufacturer
DEPUY INTERNATIONAL LTD. 8010379
Product Code
KWA
Removal / Correction Number
Z-1749/1816-2011
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
UK
Reporter Occupation
ATTORNEY

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). DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME. SHOULD THE PRODUCT AND/OR ADDITIONAL INFORMATION BE RECEIVED, THE INVESTIGATION WILL BE RE-OPENED. THE CORRECTION/REMOVAL REPORTING NUMBER LISTED APPLIES TO THE CORRESPONDING PRODUCT CODE SOLD DOMESTICALLY.

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

ASR REVISION; ASR XL - LEFT HIP; REASON FOR REVISION: UNKNOWN.

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. ASR XL - LEFT. REASON(S) FOR REVISION: UNKNOWN. (B)(4). LOT NO FOR CUP UNKNOWN ADDED COUNTRY 09 MAY 2013. UPDATE - ADDED REASON FOR REVISION, FILE HANDLER DETAILS, HOSPITAL, ADDITIONAL SURGEON, LOT NUMBER FOR CUP, ADDED HEAD BUT QUERYING INCORRECT LOT NUMBER FOR HEAD. TAKEN FROM CLAISUITE DATED 17TH MARCH 2015. REASON(S) FOR REVISION: PAIN. HOSPITAL: (B)(6) HOSPITAL. ADDITIONAL SURGEON - MR (B)(6). LOT NUMBER FOR CUP - 2459077. CORRECT LOT FOR HEAD NOW RECEIVED ON 19TH MARCH 2015.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
197124 TOTAL ASR ACET IMP SIZE 50 HIP ACETABULAR CUP KWA DEPUY INTERNATIONAL LTD. 8010379 2459077

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention