Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Hobbs Bronchial Cytology Brushes Recalled by Hobbs Medical, Inc. Due to Device was marketed for uses outside the 510(k)...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Hobbs Medical, Inc. directly.
Affected Products
Hobbs Bronchial Cytology Brushes, Model Number 4202; 4204; 4206 To be utilized by a trained physician and/or trained personnel through a flexible endoscope when brush cell samples are required for cytological analysis.
Quantity: 1820 devices
Why Was This Recalled?
Device was marketed for uses outside the 510(k) clearance.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Hobbs Medical, Inc.
Hobbs Medical, Inc. has 73 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report