Class II — Schiller, Ag
| Recalling firm | SCHILLER AG |
|---|---|
| Registered facility | SCHILLER AG (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| 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. |
| Product | Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006 |
| Quantity | 266 units |
| Distribution | US Nationwide distribution in the states of MT, WI, IL. |
| Initiated | 2025-08-08 |
| Classified | 2025-09-29 |
| Recall number | Z-2672-2025 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Schiller, Ag (Z-2672-2025).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97451/
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