UNKNOWN OXFORD BEARING
Report
- Report Number
- 3002806535-2017-00781
- Event Type
- Injury
- Date Received
- August 11, 2017
- Date of Event
- September 10, 2016
- Report Date
- August 11, 2017
- Manufacturer
- BIOMET UK LTD.
- Product Code
- JWH
- PMA / PMN Number
- PN/A
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- NL
- Reporter Occupation
- PHYSICIAN
Narratives
(B)(4). CONCOMITANT PRODUCT(S): UNKNOWN OXFORD BEARING, UNKNOWN OXFORD FEMORAL. INITIAL REPORTER MATTHIJS P. SOMFORD, REINOUD W. BROUWER, PIETER-STIJN W.A. HAEN, JOS J.A.M. VAN RAAY, AND TOM M. VAN RAAIJ ¿TECHNICAL ASPECTS OF REVISION AND FUNCTIONAL OUTCOME AFTER REVISION OF THE OXFORD UNICOMPARTMENTAL KNEE ARTHROPLASTY¿ THE KNEE 23 (2016) 1020-1023. REPORT SOURCE: (B)(6). THE REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. A DEVICE HISTORY RECORD REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. A COMPLAINT HISTORY REVIEW WAS UNABLE TO BE PERFORMED AS THE PART AND LOT NUMBERS ARE UNKNOWN. A ROOT CAUSE WAS UNABLE TO BE DETERMINED AS THE NECESSARY INFORMATION TO ADEQUATELY INVESTIGATE THE REPORTED EVENT WAS NOT PROVIDED. IF ANY FURTHER INFORMATION IS FOUND WHICH WOULD CHANGE OR ALTER ANY CONCLUSIONS OR INFORMATION, A SUPPLEMENTAL WILL BE FILED ACCORDINGLY. ZIMMER BIOMET WILL CONTINUE TO MONITOR FOR TRENDS. PRODUCT LOCATION UNKNOWN.
IT WAS REPORTED IN A JOURNAL ARTICLE THAT ELEVEN PATIENTS WERE REVISED TO ADDRESS BEARING DISLOCATIONS.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 567833 | UNKNOWN OXFORD BEARING | PROSTHESIS, KNEE | JWH | BIOMET UK LTD. | N/A | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| R |