DUROM HIP
Report
- Report Number
- 9613350-2011-00672
- Event Type
- Injury
- Date Received
- October 13, 2011
- Report Date
- September 16, 2011
- Manufacturer
- ZIMMER, INC.
- Product Code
- KWA
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- UK
- Reporter Occupation
- PHYSICIAN
Narratives
THE MFR 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. A CLEAR CORRELATION BETWEEN THE DEVELOPED METAL ALLERGY OF THE PT AND THE PRODUCT CANNOT BE RULED OUT AS IT IS ALREADY KNOWN FOR SIMILAR METAL ON DEVICES FROM LITERATURE (K. DE SMET, R. DE HANN, A. CALISTRI, P.A CAMPBELL, E. EBRAMZADEH, C. PATTYN, AND H.S. GILL. METAL ION MEASUREMENT AS A DIAGNOSTIC TOOL TO IDENTIFY PROBLEMS WITH METAL-ON-METAL HIP RESURFACING. JBJS AM 2008; 90: 202-208). OUT INVESTIGATION HAS SHOWN THAT METAL ION MEASUREMENTS FOR THE DUROM SYSTEM ARE COMPARABLE TO OTHER MOM DEVICES IN THE MARKET. AN ALLERGIC REACTION CAN BE AN INHERENT POST OPERATIVE SIDE EFFECT AS STATED IN ZIMMER'S IFU ((B)(4)). THIS IS UNFORTUNATELY PATIENT DEPENDANT AND CAN OCCUR WITH A LOW PERCENTAGE RATE WITH ALL KIND OF METAL ON METAL BASED PRODUCTS. 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 AS CLOSED. (B)(4).
IT WAS REPORTED THAT THE PT HAS A VERY HIGH COBALT LEVEL IN THE BLOOD AND IS TREATED WITH ANTIBIOTICS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 1 | DUROM HIP | DUROM ACETABULAR COMPONENT AND METASUL | KWA | ZIMMER, INC. | UNK |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Other |