Schiller, Ag: Medical Device Recall in 2025 - (Recall #: Z-2672-2025)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2025.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: August 8, 2025

Date Posted: October 8, 2025

Recall Number: Z-2672-2025

Event ID: 97451

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.

Status: Ongoing

Product Quantity: 266 units

Code Information:

REF: 1A.701307: UDI- 07613365003024 REF: 3.921002, UDI: 07613365001914 REF: 3.921030, UDI: 07613365003468 REF: 3.921031: UDI: 07613365003475 REF: 3.921006, UDI: 07613365000115 Affected Serial Numbers: 7010.000160 and lower, 7012.000356 and lower, 7013.000256 and lower, 7014.000152 and lower

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated