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Organ Recovery Systems, Inc.

Last updated September 17, 2026

Information

Country: US
Address: One Pierce Place, Itasca, IL, 60143
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PRRC Contact: —
EUDAMED SRN: —
FDA FEI Number: 3004068499
DUNS Number: —

Catalogue (26)

Device	Model / Reference	Registries	Class	Status
Kps-1®	KPS-1	FDA UDI	Class II	Active
LifePort® Kidney Transporter	LKT300	FDA UDI	Class II	Unknown
LifePort® Kidney Transporter	LKT201X	FDA UDI	Class II	Active
LifePort® Kidney Transporter	LKT300	FDA UDI	Class II	Active
SPS-1® (UW Solution)	SPS-1	FDA UDI	Class II	Active
LifePort® Kidney Transporter	LKT100P	FDA UDI	Class II	Active
LifePort® Kidney Transporter	LKT101P	FDA UDI	Class II	Active
SPS-1® (UW Solution)	SPS-1	FDA UDI	Class II	Active
LifePort® Kidney Transporter	CAN0008	FDA UDI	Class II	Active
LifePort® Kidney Transporter	LKT200X	FDA UDI	N/A	Active
LifePort® Kidney Transporter	CAN0003	FDA UDI	Class II	Active
LifePort® Kidney Transporter	UCAN0007	FDA UDI	Class II	Active
LifePort® Kidney Transporter	CAN0720	FDA UDI	Class II	Active
LifePort® Kidney Transporter	CAN1035	FDA UDI	Class II	Active
LifePort® Kidney Transporter	UCAN0005	FDA UDI	Class II	Active
LifePort® Kidney Transporter	CAN0005	FDA UDI	Class II	Active
LifePort® Kidney Transporter	UCAN0009	FDA UDI	Class II	Active
SPS-1® (UW Solution)	SPS-1	FDA UDI	Class II	Unknown
LifePort® Kidney Transporter	CAN1000	FDA UDI	Class II	Active
LifePort® Kidney Transporter	LKT201	FDA UDI	Class II	Active
LifePort® Kidney Transporter	LKT200	FDA UDI	Class II	Active
LifePort® Kidney Transporter	UCAN0003	FDA UDI	Class II	Active
Kps-I, The Kidney Perfusion Solution	K013575	FDA 510(k)	Class II	Active
Sps-1tm Static Preservation Solution, Models Sps-1-500 Ml, Sps 1-1l, Sps-1-2l	K091656	FDA 510(k)	Class II	Active
Lifeport, Kidney Perfusion Transporter (ktr)	K021362	FDA 510(k)	Class II	Active
Modification To Kps-1, Kidney Perfusion Solutiion	K022391	FDA 510(k)	Class II	Active

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FDA Recalls (2)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

Date	Recall No.	Class	Status	Reason
Jan 30, 2020	Z-1437-2020	—	terminated	Observed leakage at the sample port assembly which could potentially lead to loss of perfusion solution needed to maintain continuous machine perfusion.
Dec 14, 2016	Z-1111-2017	—	terminated	Organ preservation fluid recalled due to potential for bacterial contamination.