International safety notice
For this product, if the exterior (handle part) of the main unit has cracked, etc., it can not be sufficiently strengthened. Because of its ability, check the appearance before use, and if the cracks are confirmed, receiving safety information to discontinue use. I did. Since this may lead to separation (breakage) of the blade attachment part, we are asking for a voluntary recall to replace the affected products with countermeasures. Was decided.
Japan / PMDA Recalls · JPN · Jan 23, 2025
Key facts
| Title | For this product, if the exterior (handle part) of the main unit has cracked, etc., it can not be sufficiently strengthened. Because of its ability, check the appearance before use, and if the cracks are confirmed, receiving safety information to discontinue use. I did. Since this may lead to separation (breakage) of the blade attachment part, we are asking for a voluntary recall to replace the affected products with countermeasures. Was decided. |
|---|---|
| Regulator | Japan / PMDA Recalls |
| Country | JPN |
| Brand | Common name: Hodor laryngoscope for rigid intubation Sales name: Video laryngoscope ACE-VLS |
| Manufacturer | IMI Co., Ltd. |
| Date | Jan 23, 2025 |
| 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