FDA Adverse Event Injury Summary report: N

DUROM US ACETABAR COMPONENT 60/54 T

MDR report key: 1890039 · Received October 26, 2010

Report

Report Number
9613350-2010-00489
Event Type
Injury
Date Received
October 26, 2010
Date of Event
February 25, 2010
Report Date
September 30, 2010
Manufacturer
ZIMMER GMBH
Product Code
KWA
Removal / Correction Number
9613350-07/15/2008-001C
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
OH, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

INFO WAS FORWARDED FROM THE OWNER ESTABLISHMENT, ZIMMER, INC., WHICH MARKETS THE DEVICE IN THE U.S. THE MFR DID NOT RECEIVE EXPLANTED DEVICES, X-RAYS, OR OTHER SOURCE DOCUMENTS FOR REVIEW. WHERE LOT NUMBERS WERE RECEIVED FOR THE EXPLANTED 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 THIS EVENT IS RELATED TO THE ISSUES FOR WHICH ZIMMER IMPLEMENTED A CORRECTION IN 7/2008. 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 BY PT THAT HE UNDERWENT LEFT TOTAL HIP ARTHROPLASTY ON (B)(6) 2007. IT IS ALSO REPORTED THAT POST OP, PT EXPERIENCED PAIN AND WAS REVISED ON (B)(6) 2010.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DUROM US ACETABAR COMPONENT 60/54 T DUROMA ACETABULAR COMPONENT AND METASUL KWA ZIMMER GMBH NA 2343803

Patients

Seq Age Sex Outcome Treatment
1 55 YR Hospitalization| R