# FDA recall Z-2672-2025

> **Schiller, Ag** · Class II · device recall initiated 2025-08-08.

## Product

Argus PB-3000, Reference Numbers:  1A.701307,3.921002, 3.921030,3.921031, 3.921006

## 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.

## Distribution

US Nationwide distribution in the states of MT, WI, IL.

## Key facts

- **Recall number:** Z-2672-2025
- **Recalling firm:** Schiller, Ag
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-08-08
- **Report date:** 2025-10-08

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Baar, N/A, Switzerland

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2672-2025

## Citation

> AI Analytics. FDA recall Z-2672-2025. Retrieved 2026-07-26 from https://api.ai-analytics.org/recall/Z-2672-2025. Source: US FDA. Licensed CC0.

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