International safety notice
It has been discovered that some lots of BD Faseal IV line connection kits have incorrect expiration dates. We have decided to take measures to voluntarily recall the products from this lot.
Japan / PMDA Recalls · JPN · Oct 7, 2021
Key facts
| Title | It has been discovered that some lots of BD Faseal IV line connection kits have incorrect expiration dates. We have decided to take measures to voluntarily recall the products from this lot. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Connecting tube for infusion Sales name: BD Faseal IV line connection kit |
| Manufacturer | Nippon Becton Dickinson Co., Ltd. |
| Models | MD009, MC010, MD018, MC012, MD002, MD019, MD006, MD008, MC006, MD014, MC011, MFX2409 and 18 more |
| Date | Oct 7, 2021 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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