Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Recalled by Maquet Inc. Due to Certain pediatric arterial cannulas may have limited flexibility...
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 Inc. directly.
Affected Products
Maquet Getinge Group Pediatric Arterial Cannula Maquet Cardiopulmonary AG Kehler Strabe 31 76437 Rastatt Germany Phone +49 7222 932-0 Fax: +49 7222 932-1888 info.cp@maquet.com www.maquet.com Used to introduce blood and sterile solution to the circulation system during extracorporeal circulation procedures
Quantity: 20 devices US; 122 devices foreign
Why Was This Recalled?
Certain pediatric arterial cannulas may have limited flexibility due to an increased length of the "hardened" cannula tip.
Where Was This Sold?
This product was distributed to 2 states: MI, MN
About Maquet Inc.
Maquet Inc. has 2 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report