VANGUARD CR ILOK FEM-LT 65
Report
- Report Number
- 0001825034-2018-05459
- Event Type
- Injury
- Date Received
- August 7, 2018
- Date of Event
- February 22, 2016
- Report Date
- August 1, 2018
- Manufacturer
- ZIMMER BIOMET, INC.
- Product Code
- JWH
- PMA / PMN Number
- PK113550
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- OH, US
- Reporter Occupation
- PHYSICIAN
Narratives
(B)(4). CONCOMITANT MEDICAL PRODUCTS: VGD CRUC RET TIB BRG 11X71/75 CATALOG# 183441, LOT# UNK, BIOMET CC I-BEAM TRAY 71MM, CATALOG# 141223, LOT# UNK, SERIES (B)(6), CATALOG# 184764, LOT# UNK. 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 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 MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORTS: 0001825034-2018-05460.
IT WAS REPORTED PATIENT UNDERWENT A KNEE ARTHROPLASTY, AND SUBSEQUENTLY HAD A MANIPULATION PROCEDURE UNDER ANESTHESIA APPROXIMATELY ONE MONTH POST IMPLANTATION. ATTEMPTS HAVE BEEN MADE AND ADDITIONAL INFORMATION ON THE REPORTED EVENT IS UNAVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 600574 | VANGUARD CR ILOK FEM-LT 65 | PROSTHESIS, KNEE | JWH | ZIMMER BIOMET, INC. | N/A | NI |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | 65 YR | Hospitalization| R |