Schiller, Ag: Device Recall
Recall #Z-2672-2025 · 08/08/2025
Class II: Risk
Recall Details
- Recall Number
- Z-2672-2025
- Classification
- Class II
- Product Type
- Device
- Recalling Firm
- Schiller, Ag
- Status
- Ongoing
- Date Initiated
- 08/08/2025
- Location
- Baar, N/A, Switzerland
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 266 units
Reason for Recall
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.
Product Description
Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006
Distribution Pattern
US Nationwide distribution in the states of MT, WI, IL.
Other Recalls by Schiller, Ag
- Class II: Risk 07/24/2024
Data from FDA openFDA enforcement reports. This site is not affiliated with or endorsed by the FDA. Recall information may be updated by the FDA at any time.