INNOKAS MEDICAL OY CARESCAPE VC150 Vital Signs Monitor recall — FDA Z-2604-2016
A software error on released software versions 1.6.12, 1.6.12F and 1.6.16 may give wrong time data to measurements.
Overview of recall records associated with INNOKAS MEDICAL OY, including dates, categories and classifications where available.
Classification mix: Class II: 1.
A software error on released software versions 1.6.12, 1.6.12F and 1.6.16 may give wrong time data to measurements.
This page summarizes recall records in which the official source identifies INNOKAS MEDICAL OY as the recalling firm or manufacturer. The number of records should not be treated as a safety rating or a measure of company size, because recall counts depend on product mix, reporting periods and how government records are organized.
Compare the dates, categories and classifications together rather than relying on the total alone. Open an individual record for the recalled product, reason, distribution details and current instructions available from the source.