FDA Adverse Event Injury Summary report: N

DUROM US ACETABULAR COMPONENT 56/50 P

MDR report key: 2111763 · Received May 24, 2011

Report

Report Number
9613350-2011-00325
Event Type
Injury
Date Received
May 24, 2011
Date of Event
October 16, 2008
Report Date
May 2, 2011
Manufacturer
ZIMMER GMBH
Product Code
KWA
Removal / Correction Number
C9613350-07/15/2008-001
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
ID, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

INFO WAS FORWARDED FROM THE OWNER ESTABLISHMENT, ZIMMER, INC., WHICH MARKETS THE DEVICES IN THE (B)(6). THE MFR DID NOT RECEIVE EXPLANTED DEVICES OR X-RAYS. THE OP REPORT HAS BEEN REVIEWED. IT CONFIRMS ASEPTIC LOOSENING OF THE ACETABULAR COMPONENT. WHERE LOT NUMBERS WERE RECEIVED FOR THE EXPLANTED DEVICES, THE DEVICE HISTORY RECORDS WERE REVIEWED AND FOUND TO BE CONFORMING. IT IS NOT SUSPECTED THAT PRODUCT FAILURE LEAD TO THE ALLEGED EVENT. WHILE A CAUSE FOR THIS SPECIFIC CLINICAL EVENT CANNOT BE ASCERTAINED FROM THE INFO PROVIDED, THE COMMON CLINICAL PRESENTATION AND THE DATE OF THE ORIGINAL IMPLANTATION SUGGEST THAT THE REVISION SURGERY IS RELATED TO THE ISSUES FOR WHICH ZIMMER IMPLEMENTED A CORRECTION IN JULY 2008. SHOULD ADD'L INFO BECOME AVAILABLE AND/OR THE DEVICE(S) BE RETURNED FOR EVAL AND AN INVESTIGATION RESULT BE AVAILABLE, THAT CHANGES THIS ASSESSMENT, AN AMENDED MEDICAL DEVICE REPORT WILL BE FILED. THE NEED FOR FURTHER CORRECTIVE MEASURES IS NOT INDICATED AT THIS TIME AND ZIMMER (B)(4) CONSIDERS THIS CASE CLOSED. (B)(4).

Description of Event or Problem · 1

IT IS REPORTED THAT PT UNDERWENT RIGHT TOTAL HIP ARTHROPLASTY ON (B)(6) 2007. IT IS ALSO REPORTED POST OP, PT EXPERIENCED PAIN AND LOOSENING, AND WAS REVISED ON (B)(6) 2008.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DUROM US ACETABULAR COMPONENT 56/50 P DUROM ACETABULAR COMPONENT AND METASUL KWA ZIMMER GMBH 2357502

Patients

Seq Age Sex Outcome Treatment
1 49 YR