FDA Adverse Event Injury Summary report: N

ASR ACETABULAR CUPS 60

MDR report key: 2071498 · Received April 15, 2011

Report

Report Number
1818910-2011-06661
Event Type
Injury
Date Received
April 15, 2011
Report Date
March 16, 2011
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
CA, US
Reporter Occupation
ATTORNEY

Narratives

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

ADDITIONAL INFO: CATALOG AND LOT #. DEPUY CONSIDERS THE INVESTIGATION CLOSED AT THIS TIME.

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.

Description of Event or Problem · 1

LITIGATION PAPERS ALLEGE AFTER SURGERY, PATIENT SUFFERED SYMPTOMS AND DAMAGE TO HIS BODY INCLUDING BUT NOT LIMITED TO SEVERE PAIN AND DISCOMFORT IN HIS RIGHT THIGH, RIGHT HIP-JOINT AND GROIN; THE FORMATION OF SEVERE METALLOSIS WHICH HAS DAMAGED BONE AND TISSUE SURROUNDING THE IMPLANT; CHROMIUM AND COBALT METAL TOXICITY; LACK OF MOBILITY; AND OTHER COMPLICATIONS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 ASR ACETABULAR CUPS 60 TOTAL HIP REPLACEMENT KWA DEPUY INTERNATIONAL NA 28890916

Patients

Seq Age Sex Outcome Treatment
1 NA Required Intervention