Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Endotine Transbleph 3.5 (CFD-080-0167) Recalled by MicroAire Surgical Instruments, LLC Due to Mislabeling
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 MicroAire Surgical Instruments, LLC directly.
Affected Products
Endotine Transbleph 3.5 (CFD-080-0167)
Quantity: 29
Why Was This Recalled?
MicroAire has initiated a limited recall (29 Units)on the Endotine Transbleph 3.5 (CFD-080-0167), Lot # 285373, due to minor mislabeling ( the front label is correct, but the side label lists an incorrect part number, i.e. CFD-080-0177).
Where Was This Sold?
The product was distributed in the United States and Sweden
About MicroAire Surgical Instruments, LLC
MicroAire Surgical Instruments, LLC has 14 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report