Maquet Cardiopulmonary Gmbh recalls
Every recall we track for Maquet Cardiopulmonary Gmbh — 5 in all, from 2025–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
5 recalls since 2017.
All FDA recall records for Maquet Cardiopulmonary Gmbh since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 0 | 0 | 0 | 0 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 0 | 0 | 0 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 0 | 0 | 0 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 0 | 1 | 1 |
| 2026 (to date) | 0 | 1 | 3 | 0 | 4 |
Most common reasons for Maquet Cardiopulmonary Gmbh recalls
What to do if you have a recalled Maquet Cardiopulmonary Gmbh product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Maquet Cardiopulmonary Gmbh recalls
3 shown- Lower riskMedical device
Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK), dilator set L, Model Numbers: 701054427 (USA), 701054427 (OUS);
Maquet recalls Percutaneous Insertion Kit (PIK) L Model 701054427 due to potential failure in sterile packaging, which could compromise infection control during medical procedures.
MaquetJul 31, 2026 - Use cautionMedical device
Maquet Cardiopulmonary Gmbh recalls Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;
Maquet recalls Bubble Sensors with model 701055720 due to cable durability issues that can cause sensor errors. Affected units may display 'Ven. bubble sensor defective' or 'Ven. bubble sensor disconnected' messages.
MaquetJan 9, 2026 - UnratedMedical device
Maquet Cardiopulmonary Gmbh recalls Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.
Maquet recalls Sprinter Cart and XL Infusion Poles due to non-compliance with international labeling standards for medical devices. Affected units may not meet safety requirements.
MaquetJun 27, 2025
Maquet Cardiopulmonary Gmbh recall questions
How many recalls has Maquet Cardiopulmonary Gmbh had?
5 recalls from Maquet Cardiopulmonary Gmbh are on record with U.S. safety agencies, from 2025–2026.
What is the most recent Maquet Cardiopulmonary Gmbh recall?
Maquet Cardiopulmonary Gmbh recalls Percutaneous Insertion Kit (PIK), dilator set L, Model Numbers: 701054427 (USA), 701054427 (OUS);, dated Jul 31, 2026. Every Maquet Cardiopulmonary Gmbh recall is listed on this page, newest first.
Why are Maquet Cardiopulmonary Gmbh products recalled?
The most common reasons on record: The packaging may not consistently maintain sterile barrier integrity. (3).
What should I do if I have a recalled Maquet Cardiopulmonary Gmbh product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Maquet Cardiopulmonary Gmbh recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.