UNKNOWN NEXGEN PATELLA
Report
- Report Number
- 0001822565-2017-08081
- Event Type
- Injury
- Date Received
- November 28, 2017
- Report Date
- November 28, 2017
- Manufacturer
- ZIMMER BIOMET, INC.
- Product Code
- JWH
- PMA / PMN Number
- PNI
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- MN, US
- Reporter Occupation
- OTHER
Narratives
ZIMMER BIOMET COMPLAINT NUMBER - (B)(4).CONCOMITANT MEDICAL PRODUCTS: UNKNOWN NEXGEN RHK FEMORAL, UNKNOWN NEXGEN RHK TIBIAL TRAY, UNKNOWN NEXGEN RHK BEARING, UNKNOWN NEXGEN RHK ASSEMBLY, AND UNKNOWN NEXGEN RHK STEM. REPORT SOURCE: LITERATURE COTTINO, U., ABDEL, M. P., PERRY, K. I., MARA, K. C., LEWALLEN, D. G., & HANSSEN, A. D. (2017). LONG-TERM RESULTS AFTER TOTAL KNEE ARTHROPLASTY WITH CONTEMPORARY ROTATING-HINGE PROSTHESES. JBJS, 99(4), 324-330. REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM THE CUSTOMER. DEVICE HISTORY RECORD (DHR) REVIEW WAS UNABLE TO BE PERFORMED AS THE LOT NUMBER OF THE DEVICE INVOLVED IN THE EVENT IS UNKNOWN. ROOT CAUSE WAS UNABLE TO BE DETERMINED. 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. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001822565-2017-07360, 0001822565-2017-07361, 0001822565-2017-07362, 0001822565-2017-08079, AND 0001822565-2017-08080. NOT RETURNED TO MANUFACTURER.
THE JOURNAL ARTICLE REPORTED ONE CASE OF DVT (DEEP VEIN THROMBOSIS) OCCURRED POST-OPERATIVELY. NO FURTHER INFORMATION HAS BEEN MADE AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 842994 | UNKNOWN NEXGEN PATELLA | PROSTHEIS, KNEE | JWH | ZIMMER BIOMET, INC. | N/A | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| R |