Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Argus PB-3000 Recalled by Schiller, Ag Due to Vital sign monitoring instrument may trigger an error...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Schiller, Ag directly.
Affected Products
Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006
Quantity: 266 units
Why Was This 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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Schiller, Ag
Schiller, Ag has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report