International safety notice
We are conducting a recall because the product may contain a product that is a different size or side than what is indicated on the product label. At the time of collection, patient monitoring will be conducted for patients who have already had implanted products subject to this recall.
Japan / PMDA Recalls · JPN · Feb 20, 2023
Key facts
| Title | We are conducting a recall because the product may contain a product that is a different size or side than what is indicated on the product label. At the time of collection, patient monitoring will be conducted for patients who have already had implanted products subject to this recall. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: total knee prosthesis Brand name: Biomet Vanguard artificial knee joint system |
| Manufacturer | Zimmer Biomet LLC |
| Models | 183104, J7220427, 183126, J7220365, J7192119 |
| Date | Feb 20, 2023 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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