OXF UNI TIB TRAY SZ C RM PMA
Report
- Report Number
- 3002806535-2017-00942
- Event Type
- Injury
- Date Received
- October 13, 2017
- Date of Event
- September 13, 2017
- Report Date
- March 1, 2018
- Manufacturer
- BIOMET UK LTD.
- Product Code
- NRA
- PMA / PMN Number
- PN/A
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- IN, US
- Reporter Occupation
- PHYSICIAN
Narratives
(B)(4). THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. MULTIPLE MDR'S WERE SUBMITTED FOR THIS EVENT. PLEASE SEE REPORTS: 3002806535-2017-00941, 3002806535-2017-00943. (B)(4). CONCOMITANT MEDICAL PRODUCTS: 277325 STRYKER OP RCP 76.0 X 11.7 LOT 174879. THE 1506090 LOCKING SCREW PARTIALLY THREAD ED 5,0 MM X 9 LOT 904093. THE 159576 OXF ANAT BRG RT MD SIZE 4 PMA LOT 2115062. THE 154723 OXF UNI TIB TRAY SZ C RM PMA LOT 2070504. THE 154601 OXFORD UNI FEMORAL MD LOT 2169305. NOT RETURNED TO MANUFACTURER.
(B)(4). REPORTED EVENT WAS UNABLE TO BE CONFIRMED DUE TO LIMITED INFORMATION RECEIVED FROM CUSTOMER. DEVICE HISTORY RECORD (DHR) WAS REVIEWED AND NO DISCREPANCIES WERE FOUND. 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.
IT WAS REPORTED THE PATIENT WAS REVISED DUE TO UNKNOWN REASONS. NO PATIENT CONSEQUENCES WERE REPORTED AND NO FURTHER INFORMATION IS AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 728653 | OXF UNI TIB TRAY SZ C RM PMA | PROSTHESIS, KNEE | NRA | BIOMET UK LTD. | N/A | 2070504 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 67 YR | Hospitalization| R |