International safety notice
After checking the manufacturing process of this product, we found that the pins that make up the wrist part of some products are not caulked. It turns out it's possible. We have decided to voluntarily recall the product due to the possibility that the product may be contaminated.
Japan / PMDA Recalls · JPN · Oct 2, 2024
Key facts
| Title | After checking the manufacturing process of this product, we found that the pins that make up the wrist part of some products are not caulked. It turns out it's possible. We have decided to voluntarily recall the product due to the possibility that the product may be contaminated. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Reusable endoscopic active treatment device Sales name: HF series instrument |
| Manufacturer | Medicaroid Co., Ltd. |
| Models | 200859, 200754, 200819, 200865, AR468648, 200749, 200833 |
| Date | Oct 2, 2024 |
| 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