FDA Adverse Event Injury Summary report: N

ASR UNI FEMORAL IMPL SIZE 43

MDR report key: 2922842 · Received January 18, 2013

Report

Report Number
1818910-2013-01182
Event Type
Injury
Date Received
January 18, 2013
Report Date
January 15, 2013
Manufacturer
DEPUY INTERNATIONAL
Product Code
KWA
PMA / PMN Number
K040627
Removal / Correction Number
Z-1749/1816-2011
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
AL, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

DEPUY STILL CONSIDERS THIS 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. (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.

Description of Event or Problem · 1

LITIGATION ALLEGED THE ASR HIP WAS EXPLANTED DUE TO POTENTIAL COBALT AND/OR CHROMIUM POISONING, SEVERE PAIN, LOSS OF MOBILITY. THERE IS NO NEW INFORMATION THAT CHANGES THE OUTCOME OF THIS INVESTIGATION. **UPDATE** (B)(4) 2013 - PLAINTIFF'S PRELIMINARY DISCLOSURE FORM WAS RECEIVED, WHICH IDENTIFIED PART/LOT INFORMATION. THE COMPLAINT AND ASSOCIATED MDRS WERE UPDATED. THERE WAS NO NEW INFORMATION THAT WOULD CHANGE THE OUTCOME OF THE INVESTIGATION.

Description of Event or Problem · 1

LITIGATION ALLEGED THE ASR HIP WAS EXPLANTED DUE TO POTENTIAL COBALT AND/OR CHROMIUM POISONING, SEVERE PAIN, LOSS OF MOBILITY. THERE IS NO NEW INFORMATION THAT CHANGES THE OUTCOME OF THIS INVESTIGATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
27435 ASR UNI FEMORAL IMPL SIZE 43 FEMORAL HEAD HIP IMPLANT KWA DEPUY INTERNATIONAL 2781411

Patients

Seq Age Sex Outcome Treatment
1 Other