J&J Solutions, Inc. DBA Corvida Medical Halo Closed System Transfer Device, closed syringe recall — FDA Z-1003-2017
Product malfunction: Needle does not retract.
Overview of recall records associated with J&J Solutions, Inc. DBA Corvida Medical, including dates, categories and classifications where available.
Classification mix: Class II: 1.
Product malfunction: Needle does not retract.
This page summarizes recall records in which the official source identifies J&J Solutions, Inc. DBA Corvida Medical 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.