Medical DeviceJun 13, 2018
Hobbs Bronchial Cytology Brushes, Model Number 4202 recall — FDA Z-2052-2018
Device was marketed for uses outside the 510(k) clearance.
Class IIFDA: TerminatedHobbs Medical, Inc.
Recall history in this database
Classification mix: Class II: 73.
Understanding this recall history
This page summarizes recall records in which the official source identifies Hobbs 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.