Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Aortic Arterial Cannula 22 Fr (O.D.) Recalled by Maquet Cardiopulmonary Ag Due to This lot of arterial cannula may have been...
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 Cardiopulmonary Ag directly.
Affected Products
Aortic Arterial Cannula 22 Fr (O.D.); 23 cm (L); with 3/8-inch connector with LL, Part Number 701002246, Article Number A22-7107. For use in cardiopulmonary bypass
Quantity: 470 US
Why Was This Recalled?
This lot of arterial cannula may have been supplied with 3/8-width de-airing plugs that could break during the process of removal from the arterial cannula.
Where Was This Sold?
This product was distributed to 1 state: VA
About Maquet Cardiopulmonary Ag
Maquet Cardiopulmonary Ag has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report