FDA Adverse Event Injury Summary report: N

ASR ACETABULAR CUPS 58

MDR report key: 2233228 · Received September 2, 2011

Report

Report Number
1818910-2011-17140
Event Type
Injury
Date Received
September 2, 2011
Report Date
May 18, 2012
Manufacturer
DEPUY INTERNATIONAL
Product Code
KWA
PMA / PMN Number
PK040627
Removal / Correction Number
Z-1749/1816-2011
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NJ, US
Reporter Occupation
ATTORNEY

Narratives

Additional Manufacturer Narrative · 1

THE ASR PLATFORM WAS VOLUNTARILY RECALLED FROM THE MARKET IN (B)(6) 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.

Additional Manufacturer Narrative · 1

DEPUY STILL CONSIDERS THIS INVESTIGATON CLOSED.

Description of Event or Problem · 1

LITIGATION PAPERS ALLEGE THE FOLLOWING: FOLLOWING HIS SURGERY, PATIENT BEGAN SUFFERING FROM DISCOMFORT AND PAIN IN HIS HIP. PATIENT IS CURRENTLY IN SEVERE PAIN, AND HEARS A POPPING AND CRACKING SOUND FROM HIS HIP. HE HAS BEEN PRESCRIBED PAIN MEDICATION BY HIS PHYSICIAN.

Description of Event or Problem · 1

UPDATE: - PLAINTIFF¿S PRELIMINARY DISCLOSURE FORM WAS RECEIVED, WHICH IDENTIFIED DOB, DOI, AND PART/LOT INFORMATION. THE COMPLAINT AND ASSOCIATED MDRS WERE UPDATED. THERE WAS NO NEW INFORMATION THAT WOULD CHANGE THE OUTCOME OF THE INVESTIGATION.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ASR ACETABULAR CUPS 58 TOTAL HIP REPLACEMENT KWA DEPUY INTERNATIONAL 2550536

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention