Early Alert: Insufflation Unit Issue From Olympus
Recall Summary Olympus is recalling certain High Flow Insufflation Unit models due to software problems that could cause overpressure events. These devices are medical equipment used to deliver gas during procedures. The recall affects specific model units manufactured by Olympus.
- Recalling firm
- Early Alert
- 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
- 2026-01-22
- Status
- Ongoing
Official recall notice from FDA-MEDWATCH-RSS
Recall details on Nibble Recalls: https://trynibble.app/recalls/1f60aa61-35ad-4437-93b6-744bf96170ce