BIOMET MODULAR FINNED STEM 40MM
Report
- Report Number
- 0001825034-2019-02710
- Event Type
- Injury
- Date Received
- June 28, 2019
- Report Date
- July 25, 2019
- Manufacturer
- ZIMMER BIOMET, INC.
- Product Code
- JWH
- PMA / PMN Number
- K171054
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- GA, US
- Reporter Occupation
- PHYSICIAN
Narratives
(B)(4). UPON RECEIPT OF ADDITIONAL INFORMATION IT HAS BEEN DETERMINED THAT THE REPORTED DEVICE DID NOT CAUSE OR CONTRIBUTE TO THE EVENT.
UPON RECEIPT OF ADDITIONAL INFORMATION IT HAS BEEN DETERMINED THAT THE REPORTED DEVICE DID NOT CAUSE OR CONTRIBUTE TO THE EVENT.
(B)(4). CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION AS THE PRODUCTS REMAIN IMPLANTED. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED. . FEMORAL ITEM # 184530 LOT # 596630 , TIBIAL TRAY ITEM # 141274 LOT # 127910, PATELLA ITEM # 141357 LOT # 778860. MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2019-02708, 0001825034-2019-02709, 0001825034-2019-02711.
IT WAS REPORTED THAT A PATIENT UNDERWENT LEFT TOTAL KNEE ARTHROPLASTY APPROXIMATELY 3.5 YEARS AGO; SUBSEQUENTLY THE PATIENT IS BEING REVISED FOR UNKNOWN REASON AT A FUTURE DATE. ATTEMPTS HAVE BEEN MADE, AND NO FURTHER INFORMATION HAS BEEN PROVIDED.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 538413 | BIOMET MODULAR FINNED STEM 40MM | PROSTHESIS, KNEE | JWH | ZIMMER BIOMET, INC. | N/A | 479370 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 78 YR | Required Intervention |