Actim PROM dipstik, REF 30831ETUS recall — FDA Z-1592-2024
Interference testing has shown that the presence of personal lubricants in the vaginal specimen can interfere with the PROM test result by providing a false positive result.
Overview of recall records associated with ACTIM OY, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Interference testing has shown that the presence of personal lubricants in the vaginal specimen can interfere with the PROM test result by providing a false positive result.
This page summarizes recall records in which the official source identifies ACTIM 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.