Euro Diagnostica AB is a quantitative/qualitative enzyme-linked immunosorbent assay (ELISA) recall — FDA Z-2919-2018
Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin.
Overview of recall records associated with Euro Diagnostica AB, including dates, categories and classifications where available.
Classification mix: Class III: 4.
Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin.
Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin.
Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin.
Incorrectly labeled Manufactured by DiaSorin, The correct term should be Distributed by DiaSorin.
This page summarizes recall records in which the official source identifies Euro Diagnostica AB 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.