International safety notice
Some of the target products have been issued by overseas manufacturers due to packaging defects in individual product packaging, which may result in the sterility of the product being unable to be guaranteed. We have decided to voluntarily recall the product after receiving a report that
Japan / PMDA Recalls · JPN · May 19, 2023
Key facts
| Title | Some of the target products have been issued by overseas manufacturers due to packaging defects in individual product packaging, which may result in the sterility of the product being unable to be guaranteed. We have decided to voluntarily recall the product after receiving a report that |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: intermittent urinary catheter Brand name: MAGIC3 GO intermittent urinary catheter |
| Manufacturer | Medicon Co., Ltd. |
| Models | JUGP2965, JUGS0010, JUGP9264, GQ3276, JUGT9167, 51814, 53812G, JUGU9025, JUGR9043, 51810, JUGP9320, JUGR2031 and 41 more |
| Date | May 19, 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