FDA Adverse Event Injury Summary report: N

DUROM US ACETABULAR COMPONENT 50/44 J

MDR report key: 2091453 · Received May 4, 2011

Report

Report Number
9613350-2011-00298
Event Type
Injury
Date Received
May 4, 2011
Date of Event
February 13, 2011
Report Date
April 12, 2011
Manufacturer
ZIMMER GMBH
Product Code
KWA
Removal / Correction Number
9613350-07/15/2008-001C
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

INFO WAS FORWARDED FROM THE OWNER ESTABLISHMENT, ZIMMER INC. , WHICH MARKETS THE DEVICES IN (B)(4). THE MFR DID NOT YET RECEIVE EXPLANTED DEVICES, X-RAYS, OR OTHER SOURCE DOCUMENTS FOR REVIEW. WHERE LOT NUMBERS WERE RECEIVED FOR THE EXPLANTED DEVICES, THE DEVICE HISTORY RECORDS WERE REVIEWED AND FOUND TO BE CONFORMING. 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 (B)(6) 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 STATED THAT LEFT DUROM HIP HAS BEEN CAUSING HER PAIN WHICH LEAD TO A REVISION. IT IS ALSO REPORTED THAT DURING REVISION SURGERY, A NERVE WAS PINCHED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DUROM US ACETABULAR COMPONENT 50/44 J DUROM ACETABULAR COMPONENT AND METASUL KWA ZIMMER GMBH 2409335

Patients

Seq Age Sex Outcome Treatment
1 60 YR Hospitalization