International safety notice
Retrieval was performed because some of the blades had a blunt part, which could result in uneven skin collection and the need for additional skin collection. Masu.
Japan / PMDA Recalls · JPN · Sep 26, 2023
Key facts
| Title | Retrieval was performed because some of the blades had a blunt part, which could result in uneven skin collection and the need for additional skin collection. Masu. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Single-use dermatome blade Sales name: Dermatome Blade |
| Manufacturer | Zimmer Biomet LLC |
| Models | 66014333, 65647382, 65648460, 65972711, 65972712, 65925348, 00-8800-000-10, 65952857, 65599469, 65952858 |
| Date | Sep 26, 2023 |
| 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