Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006
Reported: October 8, 2025 Initiated: August 8, 2025 #Z-2672-2025
Product Description
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.
Details
- Recalling Firm
- Schiller, Ag
- Units Affected
- 266 units
- Distribution
- US Nationwide distribution in the states of MT, WI, IL.
- Location
- Baar, N/A
Frequently Asked Questions
What product was recalled? ▼
Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006. Recalled by Schiller, Ag. Units affected: 266 units.
Why was this product recalled? ▼
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.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on October 8, 2025. Severity: Moderate. Recall number: Z-2672-2025.
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