International safety notice
It was discovered that the foreign manufacturer of the medical device related to the product had moved its manufacturing location, and the product was transferred before the renewal procedure was completed. It turned out that they had been shipped. Since the product differs from the content of the national manufacturer registration and is a non-conforming product, we have taken voluntary recall measures for the product. I decided to do so.
Japan / PMDA Recalls · JPN · Nov 2, 2022
Key facts
| Title | It was discovered that the foreign manufacturer of the medical device related to the product had moved its manufacturing location, and the product was transferred before the renewal procedure was completed. It turned out that they had been shipped. Since the product differs from the content of the national manufacturer registration and is a non-conforming product, we have taken voluntary recall measures for the product. I decided to do so. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Gravity drop needleless infusion set Brand name: BD natural drip infusion set for piggy |
| Manufacturer | Nippon Becton Dickinson Co., Ltd. |
| Models | NT-890, 200cm, 150cm, 08372, 08417, 08469, 08373, 08470, NT-54 |
| Date | Nov 2, 2022 |
| 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