FDA Adverse Event Injury Summary report: N

DUROM US ACETABAR COMPONENT 56/50 P

MDR report key: 1770116 · Received July 7, 2010

Report

Report Number
9613350-2010-00337
Event Type
Injury
Date Received
July 7, 2010
Report Date
May 24, 2010
Manufacturer
ZIMMER GMBH
Product Code
KWA
Removal / Correction Number
9613350-07/15/2008-001C
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
NY, US
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

INFO WAS FORWARDED FROM THE OWNER ESTABLISHMENT, ZIMMER INC., WHICH MARKETS THE DEVICES IN THE U.S. THE MANUFACTURER DID NOT 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 JULY 2008. SHOULD ADDITIONAL 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 TOTAL HIP REPLACEMENT ON (B) (6) 2007, IN WHICH HE RECEIVED A DUROM CUP ACETABULAR COMPONENT. POST-OP, PT HAS BEEN EXPERIENCING PAIN AND HIS DOCTOR HAS RECOMMENDED REVISION, WHICH IS NOT YET SCHEDULED.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 DUROM US ACETABAR COMPONENT 56/50 P DUROM ACETABULAR COMPONENT AND METASUL KWA ZIMMER GMBH NA 2349670

Patients

Seq Age Sex Outcome Treatment
1 68 YR Hospitalization