Class IIOngoingZ-3146-2026
Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK)
The packaging may not consistently maintain sterile barrier integrity.
Maquet Cardiopulmonary…Sep 23, 2026
Maquet Cardiopulmonary Gmbh recalls
Drawn from openFDA device enforcement reports. Filter by severity, status, state, year, or manufacturer.
Showing 1–5 of 5 recalls
Class IIOngoingZ-3145-2026
Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK)
The packaging may not consistently maintain sterile barrier integrity.
Maquet Cardiopulmonary…Sep 23, 2026
Class IIOngoingZ-3144-2026
Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK)
The packaging may not consistently maintain sterile barrier integrity.
Maquet Cardiopulmonary…Sep 23, 2026
Class IIOngoingZ-1300-2026
Maquet Cardiopulmonary Gmbh recalls Bubble Sensor for 3/8" x 3/32" tubing
Internal investigations have identified an issue with the durability of the connecting cable near the connection to the Venous Bubble Sensor.…
Maquet Cardiopulmonary…Feb 11, 2026
Class IIOngoingZ-2193-2025
Maquet Cardiopulmonary Gmbh recalls Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion…
Device does not comply with the labeling requirements of international standard IEC 60601-1.
Maquet Cardiopulmonary…Aug 6, 2025