International safety notice
Regarding our kit product, we have received a report from a customer that the type of catheter connector, which is one of the components, is different. We received it from Mr. It was confirmed that the following data (old standard product) were incorporated and mixed together. We have decided to carry out a voluntary recall of the affected products.
Japan / PMDA Recalls · JPN · Jul 20, 2021
Key facts
| Title | Regarding our kit product, we have received a report from a customer that the type of catheter connector, which is one of the components, is different. We received it from Mr. It was confirmed that the following data (old standard product) were incorporated and mixed together. We have decided to carry out a voluntary recall of the affected products. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Delivery anesthesia catheter Brand name: Perifix catheter |
| Manufacturer | B.Brown Ace Scrap Co., Ltd. |
| Models | 21B11A8701, 4515048N-01 |
| Date | Jul 20, 2021 |
| 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