Overview of recall records associated with Bioporto Diagnostics A/S, including dates, categories and classifications where available.
Classification mix: Class II: 1.
The use of a non-validated rework process for assay reagents which could lead to missed diagnosis of renal disease, inappropriate treatment decisions, or inappropriate monitoring of renal…
This page summarizes recall records in which the official source identifies Bioporto Diagnostics A/S 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.
