Reported Oct 8, 2025 · Ongoing
Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006
Schiller, Ag
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Schiller, Ag · Altgasse 68 · Baar, N/A · N/A
Is this the product you have?
- Argus PB-3000
- Reference Numbers
1A.7013073.9210023.9210303.9210313.921006
- Lot codes and dates
5 of 5 products
Products covered by this recall Model / number Barcodes Product as published 1A.70130707613365003024UDI- 07613365003024 3.92100207613365001914UDI: 07613365001914 3.92103007613365003468UDI: 07613365003468 3.92103107613365003475UDI: 07613365003475 3.92100607613365000115UDI: 07613365000115 Affected Serial Numbers: 7010.000160 and lower, 7012.000356 and lower, 7013.000256 and lower, 7014.000152 and lower - Amount recalled
- 266 units
Where it was sold
Why it was 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.
This product could cause temporary or reversible health problems — stop using it.
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