Overview of recall records associated with Magnolia Medical Technologies, Inc., including dates, categories and classifications where available.
Classification mix: Class II: 2.
Due to an uptick of complaints associated with premature needle retraction of blood collection system.
Product was shipped with the incorrect Transfer Adapter Instructions For Use (IFU).
This page summarizes recall records in which the official source identifies Magnolia Medical Technologies, 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.
