Class II — Potential Health Hazard

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...

Date: June 27, 2025
Company: Maquet Cardiopulmonary Gmbh
Status: Ongoing
Source: FDA (Device)

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.

Affected (51 states)Not affected

About Maquet Cardiopulmonary Gmbh

Maquet Cardiopulmonary Gmbh has 2 total recalls tracked by RecallDetector.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report