DUROM US ACETABULAR COMPONENT 50/44 J
Report
- Report Number
- 9613350-2011-00391
- Event Type
- Injury
- Date Received
- June 16, 2011
- Date of Event
- March 1, 2011
- Report Date
- May 19, 2011
- Manufacturer
- ZIMMER GMBH
- Product Code
- KWA
- Removal / Correction Number
- C9613350-07/15/2008-001
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- DE, US
- Reporter Occupation
- PHYSICIAN
Narratives
INFO WAS FORWARDED FROM THE OWNER ESTABLISHMENT, ZIMMER, INC., WHICH MARKETS THE DEVICES IN THE UNITED STATES. THE MFR DID NOT RECEIVE EXPLANTED DEVICES. THE OPERATION REPORT HAS BEEN PROVIDED. IT CONFIRMS ASEPTIC LOOSENING OF THE ACETABULAR CUP. 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)(4) 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 GMBH CONSIDERS THIS CASE CLOSED. (B)(4).
IT IS REPORTED THAT PT UNDERWENT LEFT TOTAL HIP ARTHROPLASTY ON (B)(6) 2008. IT IS ALSO REPORTED POST OP, PT EXPERIENCED PAIN AND LOOSENING, AND WAS REVISED ON (B)(6) 2011.
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 | 2325889 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization |