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Paragonix SherpaPak Cardiac Transport System

Paragonix Technologies Inc · Model SHRP-1001-000-002 · UDI-DI 00869582000361

MSB Prescription
10
510(k) clearances
73
Adverse events (15 deaths)
2
Recalls
15
Facilities

Description

Paragonix SherpaPak Cardiac Transport System HC 18mm

Recalls

DateFirmReason
2025-03-13INSTITUT GEORGES LOPEZThe potential for risk of microbiological contamination of products due to inability to ensure sterility assurance throughout aseptic manufacturing.
2011-05-12Vitrolife, Inc.Precipitation observed in some bottles of Tham buffer used for adjusting pH of Perfadex prior to perfusion of donor lungs.

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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.