Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold Recalled by Maquet Cardiopulmonary Gmbh Due to Device does not comply with the labeling requirements...
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 Gmbh directly.
Affected Products
Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.
Quantity: 7,754 units
Why Was This Recalled?
Device does not comply with the labeling requirements of international standard IEC 60601-1.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Maquet Cardiopulmonary Gmbh
Maquet Cardiopulmonary Gmbh 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