Urgent Field Safety Notice For Elisa 300, Elisa 500, Elisa 600, Elisa 800 (vit) By Löwenstein Medical Gmbh & Co. Kg
Recall Summary Löwenstein Medical is recalling elisa 300, 500, 600, and 800 (VIT) ventilation devices distributed in Germany and the EU due to an unspecified safety issue classified as Class I (the most serious level). The notice does not detail the specific hazard or risk these devices pose to patients.
- Recalling firm
- Löwenstein Medical GmbH & Co. KG
- Product
- elisa 300, elisa 500, elisa 600, elisa 800 (VIT)
- Reason
- Urgent Field Safety Notice for elisa 300, elisa 500, elisa 600, elisa 800 (VIT) by Löwenstein Medical GmbH & Co. KG
- Classification
- Class I
- Category
- medical device recall
- Country
- Germany
- Agency
- BFARM
- Recall date
- 2026-08-26
- Status
- Ongoing
- Distribution
- Germany / EU
Official recall notice from BFARM
Recall details on Nibble Recalls: https://trynibble.app/recalls/05309dad-252e-43d5-b75d-6cf1b69b5e10