International safety notice
Regarding "Aion Acti-PRP" manufactured and sold by EPJ Medical Service Co., Ltd., the stock of the distributor is Regarding some of the content in the explanation of the product on the homepage of the company Aon International, However, the expressions used were such that there was a risk of discrepancy between the certification matters and the customer's understanding. To avoid the use of this product, we will carry out a voluntary recall of products shipped to the market.
Japan / PMDA Recalls · JPN · Apr 14, 2022
Key facts
| Title | Regarding "Aion Acti-PRP" manufactured and sold by EPJ Medical Service Co., Ltd., the stock of the distributor is Regarding some of the content in the explanation of the product on the homepage of the company Aon International, However, the expressions used were such that there was a risk of discrepancy between the certification matters and the customer's understanding. To avoid the use of this product, we will carry out a voluntary recall of products shipped to the market. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | General name: Vacuum sealed blood collection tube Brand name: Aon Acti-PRP |
| Manufacturer | EPJ Medical Service Co., Ltd. |
| Models | A200014, A210005, A210014, A200017, A200021 |
| Date | Apr 14, 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