International safety notice
As a result of an investigation based on information from medical institutions, we found that the tip of the venous needle's cutting edge was slightly deformed, and the penetration resistance value deviated from internal standards. It has been discovered that a defective product is being shipped. We have decided to carry out a voluntary recall as there is a possibility that some of the shipped products may contain products in a similar condition. Ta.
Japan / PMDA Recalls · JPN · May 2, 2022
Key facts
| Title | As a result of an investigation based on information from medical institutions, we found that the tip of the venous needle's cutting edge was slightly deformed, and the penetration resistance value deviated from internal standards. It has been discovered that a defective product is being shipped. We have decided to carry out a voluntary recall as there is a possibility that some of the shipped products may contain products in a similar condition. Ta. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Single-use general venous winged needle Brand name: Terumo Winged Intravenous Needle |
| Manufacturer | Terumo Corporation |
| Models | 220127B, SV-25DLK, SV-23DLK, 220121B／220124B／220205B |
| Date | May 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