International safety notice
The fiber metal pad may not be properly welded to this product, so it will be recalled.
Japan / PMDA Recalls · JPN · Apr 5, 2024
Key facts
| Title | The fiber metal pad may not be properly welded to this product, so it will be recalled. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Prosthetic knee femoral component Sales name: NexGen CR-FLEX Porous Femoral |
| Manufacturer | Zimmer Biomet LLC |
| Models | 64242244, 64254387, 00-5952-015-02, 65038150, 64261035, 64540917, 64261032, 64808858, 64808878, 00-5952-015-05, 64275538, 64827305 and 118 more |
| Date | Apr 5, 2024 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
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