Schiller, Ag FDA Recalls

2 recalls on file across devices, 0 of them Class I and 2 still open. This firm is not matched to a listed company.

Newest first

Class I is the FDA's most serious grade: a reasonable probability of serious harm or death.

Product	Reason	Class	Initiated
Argus PB-3000, Reference Numbers: 1A.701307,3.921002, 3.921030,3.921031, 3.921006Class IIAug 8, 2025Vital sign monitoring instrument may trigger an error messag	Vital sign monitoring instrument may trigger an error message during blood pressures measurements, Specifical	Class IIDevices	Aug 8, 2025
CARDIOVIT AT-180. Model Number: 0A.110000; Catalog number: 3.920570Class IIJul 24, 2024Potential for high-frequency signal artifacts is recorded du	Potential for high-frequency signal artifacts is recorded during an ECG acquisition performed by CARDIOVIT AT-	Class IIDevices	Jul 24, 2024