BASE 10 GENETICS RNAstill Molecular Transport Medium Vial, Catalog number MTM-001, a recall — FDA Z-0568-2022
The product does not have 510(k) clearance.
Overview of recall records associated with BASE 10 GENETICS Inc., including dates, categories and classifications where available.
Classification mix: Class I: 1.
The product does not have 510(k) clearance.
This page summarizes recall records in which the official source identifies BASE 10 GENETICS Inc. 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.