Maquet Cardiopulmonary recalls
4 official recalls and safety alerts involving Maquet Cardiopulmonary since 2025-06, from FDA · Device. Newest first. Check the official notice for exact models and batch codes.
This list only includes recalls Recall Atlas has collected since 2021-10. A product not listed here may still be affected; check with Maquet Cardiopulmonary or the relevant agency.
- 2026-09-23
USMaquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK), Guidewire 100 cm, Model Numbers: 701053068 (USA), 701047384 (OUS);
The packaging may not consistently maintain sterile barrier integrity.
FDA · DeviceMaquet Cardiopulmonary GmbhWorldwide distribution - US Nationwide and the countries of Australia,…Official notice →- 2026-02-11
- US
Maquet Cardiopulmonary Gmbh recalls Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;
Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Venous Bubble Sensor. Excessive bending of the connecting cable can lead to full damage of the…
FDA · DeviceMaquet Cardiopulmonary GmbhWorldwide Distribution: US (Nationwide) and OUS (International) to countries…Official notice → - 2025-08-06
- US
Maquet Cardiopulmonary Gmbh recalls Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.
Device does not comply with the labeling requirements of international standard IEC 60601-1.
FDA · DeviceMaquet Cardiopulmonary GmbhWorldwide distribution - US Nationwide and the countries of Australia, New…Official notice → - 2025-06-04
- US
Maquet Cardiopulmonary Ag recalls Cardiohelp System HKH 8820 Wall Holder. Mounting bracket designed to hold the CARDIOHELP-i system for interhospital transport by…
HKH 8820 Wall Holder does not comply with standard DIN EN 1789:20 and has the potential to detach.
FDA · DeviceMaquet Cardiopulmonary AgDomestic: IL & MO. Foreign: Australia, Austria, Belgium, Canada, China,…Official notice →