International safety notice
When I opened the package from the seller to use the circuit at a medical institution, it actually contained two types of attachments (LM-15, infusion line). When I was supposed to, I was informed that two of the same attached items (LM-15) were included. As a result of the investigation, we determined that a recall is necessary as we cannot deny the possibility that there are multiple cases of similar attachments being misplaced on the market. did.
Japan / PMDA Recalls · JPN · Jul 25, 2023
Key facts
| Title | When I opened the package from the seller to use the circuit at a medical institution, it actually contained two types of attachments (LM-15, infusion line). When I was supposed to, I was informed that two of the same attached items (LM-15) were included. As a result of the investigation, we determined that a recall is necessary as we cannot deny the possibility that there are multiple cases of similar attachments being misplaced on the market. did. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | General name: Blood circuit for plasma separation Brand name: Plasmapheresis therapy circuit |
| Manufacturer | Naniwa Rubber Industry Co., Ltd. |
| Models | 190397, 120set, PT-2020D |
| Date | Jul 25, 2023 |
| 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