Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
AXIUS Blower Mister Product Code/REF Number: CB-1000 The Axius Blower Recalled by Maquet Cardiovascular, LLC Due to Potential lack of carbon dioxide (CO2) flow that...
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 Maquet Cardiovascular, LLC directly.
Affected Products
AXIUS Blower Mister Product Code/REF Number: CB-1000 The Axius Blower Mister is intended to clear an anastomotic site for improved visibility
Quantity: 7,880 each (1,576 packs of 5)
Why Was This Recalled?
Potential lack of carbon dioxide (CO2) flow that may result in a procedural delay during off-pump coronary artery bypass (OPCAB).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Maquet Cardiovascular, LLC
Maquet Cardiovascular, LLC has 251 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report