OSS POLY TIBIAL BUSHING
Report
- Report Number
- 0001825034-2021-01222
- Event Type
- Injury
- Date Received
- April 23, 2021
- Date of Event
- March 12, 2019
- Report Date
- June 3, 2021
- Manufacturer
- ZIMMER BIOMET, INC.
- Product Code
- JDI
- UDI-DI
- 00880304002258
- PMA / PMN Number
- K002757
- Removal / Correction Number
- N/A
- Adverse Event
- Yes
- Product Problem
- Yes
- Report Source
- Manufacturer report
- Reporter Location
- TX, US
- Reporter Occupation
- PHYSICIAN
Narratives
THIS FOLLOW-UP IS BEING SUBMITTED TO RELAY ADDITIONAL INFORMATION. NO PRODUCT WAS RETURNED OR PICTURES PROVIDED; THEREFORE, VISUAL AND DIMENSIONAL EVALUATIONS COULD NOT BE PERFORMED. MEDICAL RECORDS WERE NOT PROVIDED. DEVICE HISTORY RECORD (DHR) WAS REVIEWED FOR DEVIATIONS AND/ OR ANOMALIES WITH NO RELATED DEVIATIONS / ANOMALIES IDENTIFIED. A DEFINITIVE ROOT CAUSE CANNOT 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.
NO FURTHER EVENT INFORMATION AVAILABLE AT THE TIME OF THIS REPORT.
(B)(4). MULTIPLE MDR REPORTS WERE FILED FOR THIS EVENT, PLEASE SEE ASSOCIATED REPORT: 0001825034-2021-01217, 0001825034-2021-01218, 0001825034-2021-01219, 0001825034-2021-01220, 0001825034-2021-01221, 0001825034-2021-01223, 0001825034-2021-01224, 0001825034-2021-01225, 0001825034-2021-01226. MEDICAL PRODUCT: OSS REINFORCED YOKE, ITEM#: 150493, LOT#: 211420. OSS TIBIAL POLY BEARING 20MM, ITEM#: 150414, LOT#: 237060. OSS POLY LOCK PIN, ITEM#: 150478, LOT#: 348850. OSS NON-MOD TIB PLATE SHORT 67, ITEM#: 150417, LOT#: 203610. OSS 7CM SEGMENTAL FEMORAL RT, ITEM#: 150354, LOT#: 756200. OSS POLY FEMORAL BUSHINGS, ITEM#: 150477, LOT#: 370100. OSS AXLE, ITEM# :150480 , LOT#: 543370. OSS REINFORCED YOKE, ITEM#: 150493 , LOT#: 658130. OSS TIBIAL POLY BEARING 22MM, ITEM#: 150415, LOT#: 382120. OSS 3CM ELLIP DIAPHYSEAL SEG, ITEM#: 150461, LOT#: 150610. OSS CEMENTED IM STEM 15MMX90MM, ITEM#: 150363, LOT#: 810360. CUSTOMER HAS INDICATED THAT THE PRODUCT WILL NOT BE RETURNED TO ZIMMER BIOMET FOR INVESTIGATION. THE INVESTIGATION IS IN PROCESS. ONCE THE INVESTIGATION HAS BEEN COMPLETED, A FOLLOW-UP MDR WILL BE SUBMITTED.
IT WAS REPORTED THAT A PATIENT WAS REVISED APPROXIMATELY TWO MONTHS¿ POST IMPLANTATION DUE TO WOUND HEALING PROBLEMS THAT DISENGAGED HIS HINGED FEMUR FROM HIS RIGHT TIBIAL COMPONENT. THIS WAS A RESULT OF HAVING HAD A DISTAL FEMORAL REPLACEMENT WITH ABSENCE OF COLLATERAL LIGAMENTS CAUSING THE FEMUR TO DISENGAGE FROM THE TIBIA WHEN THE KNEE BECAME FLEXED. ATTEMPTS TO OBTAIN ADDITIONAL INFORMATION HAVE BEEN MADE; HOWEVER, NO MORE INFORMATION IS AVAILABLE.
Devices
| Seq | Brand | Generic | Product Code | Manufacturer | Model | Lot | UDI-DI |
|---|---|---|---|---|---|---|---|
| 609446 | OSS POLY TIBIAL BUSHING | PROSTHESIS, HIP | JDI | ZIMMER BIOMET, INC. | N/A | 460720 | 00880304002258 |
Patients
| Seq | Age | Sex | Outcome | Treatment |
|---|---|---|---|---|
| 1 | Hospitalization| R |