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LILLIPUT

SORIN GROUP ITALIA SRL · Model D901 CLOSED · UDI-DI 08033178100267

DTZ Prescription
10
510(k) clearances
10,612
Adverse events (449 deaths)
107
Recalls
34
Facilities

Recalls

DateFirmReason
2025-09-12Medtronic Perfusion SystemsMedtronic identified an Affinity NT Oxygenator unit with decreased CO2 gas transfer rates that did not meet performance requirements.
2024-01-16Maquet Medical Systems USAThe Emergency Priming Line, a component of the HLS Set, may have a compromised sterile barrier due to nonconformities at the bag seal. This issue may result in inflammation, sepsis
2024-01-16Maquet Medical Systems USAThe Emergency Priming Line, a component of the HLS Set, may have a compromised sterile barrier due to nonconformities at the bag seal. This issue may result in inflammation, sepsis
2023-05-18Maquet Medical Systems USA1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and c
2023-05-18Maquet Medical Systems USA1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and c
2023-05-18Maquet Medical Systems USA1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and c
2023-05-18Maquet Medical Systems USAProduct packaging may exhibit small pinholes which may not be visible to the unaided eye, compromising the sterile barrier of the packaging. Exposure to non-sterile device may resu
2023-05-18Maquet Medical Systems USA1. An accessory may be improperly placed during packaging, causing creases and damage to the accessory's sterile pouch. 2. Product packaging may exhibit holes, cracks, dents, and c
2023-05-18Maquet Medical Systems USAProduct packaging may exhibit small pinholes which may not be visible to the unaided eye, compromising the sterile barrier of the packaging. Exposure to non-sterile device may resu
2023-05-18Maquet Medical Systems USAProduct packaging may exhibit small pinholes which may not be visible to the unaided eye, compromising the sterile barrier of the packaging. Exposure to non-sterile device may resu

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.