FDANovember 23, 2023device
Actim PROM dipstik, REF 30831ETUS; qualitative immunoassay rapid test for rupture of fetal membrane
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
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.
What to do
FDA enforcement status: Ongoing
Brands named
actim oyactim
UPCs
06430030990608
Recall history
No related federal recalls on record for this brand yet.
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