International safety notice
Common names: (1)-(5) Total knee prosthesis (6) Total knee prosthesis tibial component* Brand name: (1) Optetrac artificial knee joint (2) Optetrack LogicPS artificial knee joint system (3) Optetrack LogicCR artificial knee joint system (4) Truliant PS artificial knee joint system (5) Truliant CR artificial knee joint system (6) Optetrack CR slope tibial insert*
Japan / PMDA Recalls · JPN · Oct 18, 2022
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | Common names: (1)-(5) Total knee prosthesis (6) Total knee prosthesis tibial component* Brand name: (1) Optetrac artificial knee joint (2) Optetrack LogicPS artificial knee joint system (3) Optetrack LogicCR artificial knee joint system (4) Truliant PS artificial knee joint system (5) Truliant CR artificial knee joint system (6) Optetrack CR slope tibial insert* |
| Manufacturer | Exact Tech Co., Ltd. |
| Models | 2615944, 2725488, 1823185, 2279921, 1698094, 6267038, 6158648, 1505624, 1513897, 2665696, 200-22-09, 2531314 and 17876 more |
| Date | Oct 18, 2022 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1