Baar, Switzerland
Schiller, Ag recalls
2 recalls recorded since 2018, most recently on 8 August 2025. 2 are listed as ongoing. Status and classification are as published by the FDA.
Recalls2
Ongoing (FDA)2
Terminated or completed0
Class I (FDA)0
Ongoing Class II Medical devices
- Recall started
- 8 August 2025
- Reason
- Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifically, when the initial inflation pressure is set in the high-pressure range.
- Distribution
- US Nationwide distribution in the states of MT, WI, IL.
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2672-2025
- Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006
Ongoing Class II Medical devices
- Recall started
- 24 July 2024
- Reason
- Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-180 electrocardiographs.
- Distribution
- Worldwide - US distribution in the state of Florida and the countries of Austria, Belgium, Switzerland, Cyprus, Czechia, Germany, Spain, Finland, France, Great Britain, Ireland, Iceland, Italy, Luxembourg, Malta, The Netherlands, Norway, Portugal, Romania, Sweden, Slovenia, Australia, The United Ara
- Initiated
- Voluntary: Firm initiated
- Recall number
- Z-2734-2024
- CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570
A terminated FDA recall means the FDA has determined that all reasonable efforts to remove or correct the product have been made. What statuses mean.