Overview of recall records associated with Angiodynamics Inc. (Navilyst Medical Inc.), including dates, categories and classifications where available.
Classification mix: Class II: 1.
Mislabeled: The product is labeled as 5F (55cm; Maximum Flow Rate 3.5 mL/Sec) and the product is actually 4F (55cm; Maximum Flow Rate 3.5 mL/Sec).
This page summarizes recall records in which the official source identifies Angiodynamics Inc. (Navilyst Medical 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.
