Insufflation Unit Recall: Olympus Removes High Flow Insufflation Units
Olympus is recalling certain High Flow Insufflation Unit models due to software problems that could cause the device to deliver excessive pressure. These units are medical devices used during procedures to inflate body cavities. The recall affects specific insufflation unit models made by Olympus.
- Recalling firm
- Insufflation Unit Recall
- Product
- Olympus is removing certain High Flow Insufflation Unit models due to software issues that may lead to overpressure events.
- Reason
- Olympus is removing certain High Flow Insufflation Unit models due to software issues that may lead to overpressure events.
- Category
- consumer product recall
- Country
- United States
- Agency
- FDA-MEDWATCH-RSS
- Recall date
- 2026-02-23
- Status
- Ongoing
Official recall notice from FDA-MEDWATCH-RSS
Recall details on Nibble Recalls: https://trynibble.app/recalls/bbacbc8e-3a1f-4991-8ea3-f0d957581343