Organ Recovery Systems, Inc.
Organ Recovery Systems, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2010, with 2 FDA device recalls on record.
Top product codes for Organ Recovery Systems, Inc.
FDA recalls by Organ Recovery Systems, Inc.
- Z-1437-2020 — LKT200 Perfusion Circuit, part of Lifeport Kidney Perfusion Transporter KTR - Product Usage: The circuit is an accessory to LifePort Kidney Perfusion Transporter (KTR) Isolated kidney perfusion and transport system, which is intended to be used for the continuous hypothermic machine perfusion of kidneys for the preservation, transportation and eventual transplantation into a recipient.
- Z-1111-2017 — SPS-1, Static Preservation Solution [1 or 2 liter bags], Sterile; Organ Recovery Systems, One Pierce Place, Itasca, IL 60143
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Organ Recovery Systems, Inc.
Data sourced from openFDA. This site is unofficial and independent of the FDA.