FDA Adverse Event Injury Summary report: N

TOTAL ASR FEM IMP SIZE 46

MDR report key: 3061438 · Received April 16, 2013

Report

Report Number
1818910-2013-04791
Event Type
Injury
Date Received
April 16, 2013
Date of Event
March 23, 2009
Report Date
December 11, 2013
Manufacturer
DEPUY INTERNATIONAL
Product Code
KXA
Removal / Correction Number
Z-1749/1816-2011
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED.

Additional Manufacturer Narrative · 1

DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED.

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. REF. (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

DEPUY STILL CONSIDERS THE INVESTIGATION CLOSED.

Description of Event or Problem · 1

ASR REVISION; ASR RESURFACING - RIGHT HIP; REASON FOR REVISION: UNKNOWN.

Description of Event or Problem · 1

REASON FOR REVISION: DISLOCATION.

Description of Event or Problem · 1

ADDITIONAL REASON FOR REVISION: DISCLOCATIONS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
161919 TOTAL ASR FEM IMP SIZE 46 ASR TOTAL HIP REPLACEMENT KXA DEPUY INTERNATIONAL 2350600

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention