--- title: "Maquet Cardiopulmonary Gmbh Recalls: Agency-Reported Status and History (Oct 1, 2026) | Is It on Recall" description: "Search Maquet Cardiopulmonary Gmbh recall records, lots, firms and dates. Reported status can be incomplete; use the linked agency notice for current instructions." url: https://isitonrecall.com/brand/maquet-cardiopulmonary-gmbh/ updated: 2026-10-01 site: "Is It on Recall" language: en --- [Home](https://isitonrecall.com/) / Brand archive # Maquet Cardiopulmonary Gmbh recall records **5** reported ongoing 5 records in this archive. Latest source date Jul 31, 2026. FDA enforcement status can lag behind the recall lifecycle. An empty search or a reported termination is not a personal product-safety determination. Archive changed Oct 1, 2026. USDA FSIS records are unavailable; [check FSIS directly](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/). ## Records and reported status Jul 31, 2026 FDA device enforcement ### [Percutaneous Insertion Kit (PIK), Guidewire 100 cm, Model Numbers: 701053068 (USA), 701047384 (OUS);](https://isitonrecall.com/recall/fda-device-z-3144-2026-percutaneous-insertion-kit-pik-guidewire-100-cm-model-numbers-701053068-usa-701047384-ous/) The packaging may not consistently maintain sterile barrier integrity. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belarus, Belgium, Brazil, Canada, China, Colombia, Czech Republic, Denmark, Finland, France, Germ... [Official source for Percutaneous Insertion Kit (PIK), Guidewire 100 cm, Model Numbers: 701053068 (USA), 701047384 (OUS);](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3144-2026%22) Jul 31, 2026 FDA device enforcement ### [Percutaneous Insertion Kit (PIK), Guidewire 150 cm, Model Numbers: 701053069 (USA), 701047385 (OUS);](https://isitonrecall.com/recall/fda-device-z-3145-2026-percutaneous-insertion-kit-pik-guidewire-150-cm-model-numbers-701053069-usa-701047385-ous/) The packaging may not consistently maintain sterile barrier integrity. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belarus, Belgium, Brazil, Canada, China, Colombia, Czech Republic, Denmark, Finland, France, Germ... [Official source for Percutaneous Insertion Kit (PIK), Guidewire 150 cm, Model Numbers: 701053069 (USA), 701047385 (OUS);](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3145-2026%22) Jul 31, 2026 FDA device enforcement ### [Percutaneous Insertion Kit (PIK), dilator set L, Model Numbers: 701054427 (USA), 701054427 (OUS);](https://isitonrecall.com/recall/fda-device-z-3146-2026-percutaneous-insertion-kit-pik-dilator-set-l-model-numbers-701054427-usa-701054427-ous/) The packaging may not consistently maintain sterile barrier integrity. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, Austria, Belarus, Belgium, Brazil, Canada, China, Colombia, Czech Republic, Denmark, Finland, France, Germ... [Official source for Percutaneous Insertion Kit (PIK), dilator set L, Model Numbers: 701054427 (USA), 701054427 (OUS);](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-3146-2026%22) Jan 9, 2026 FDA device enforcement ### [Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;](https://isitonrecall.com/recall/fda-device-z-1300-2026-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 Venous Bubble Sensor or loose cable contac... Class II Reported ongoing Distribution: Worldwide Distribution: US (Nationwide) and OUS (International) to countries of: Albania, Algeria, Argentina, Australia, Austria, Azerbaijan, Bahrain, Belgium, Bosnia and Herzeg... [Official source for Bubble Sensor for 3/8" x 3/32" tubing; Model Number: 701055720;](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-1300-2026%22) Jun 27, 2025 FDA device enforcement ### [Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.](https://isitonrecall.com/recall/fda-device-z-2193-2025-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. Class II Reported ongoing Distribution: Worldwide distribution - US Nationwide and the countries of Australia, New Zealand, Canada, Hong Kong, India, Israel, Japan, Singapore, South Korea, Taiwan, Thailand, Austria, B... [Official source for Sprinter Cart/Sprinter Cart XL Infusion Pole. Component used to hold 2 x 2 kg infusion bags.](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-2193-2025%22) ## Reasons in these listed records - The packaging may not consistently maintain sterile barrier integrity. - 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 Venous Bubble Sensor or loose cable contact, which may trigger... - Device does not comply with the labeling requirements of international standard IEC 60601-1. These examples come from this result page and are not a ranking of every recall reason. ## Checking Maquet Cardiopulmonary Gmbh ### Is there a recall on maquet cardiopulmonary gmbh right now? This archive contains 5 records, including 5 with agency-reported ongoing status. The status field can be incomplete or stale. Open the current official notice and match your exact product. ### How do I check my package or product? Compare the product, firm and lot, date, model or serial identifiers with the notice. [Use the label-check guide](https://isitonrecall.com/guides/read-lot-codes/) if you need help locating an identifier. ### Does a matching name mean every item is included? A name is a search match. The agency notice sets the affected products and identifiers. Do not assume that every item with the same name or brand belongs to the recall. ### What if the search finds no matching record? This search has source and keyword limits. Missing records or a missing lot code do not establish that a product is unaffected. [Check source coverage](https://isitonrecall.com/sources/) and the agency's current notices. ### Where can I find older records? Use [monthly archives](https://isitonrecall.com/archives/) or the local search. The initial import covers records dated from October 2021 where available; each source's actual first and latest dates appear on the coverage page. ## Keep checking [Search Maquet Cardiopulmonary Gmbh](https://isitonrecall.com/check/?q=Maquet%20Cardiopulmonary%20Gmbh) [Browse related products](https://isitonrecall.com/products/) [Review source dates](https://isitonrecall.com/sources/)