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Sentinel®

ALCOR SCIENTIFIC INC. · Model S-1000-SI · UDI-DI 00896406002355

LZH

510(k) clearances

14,912

Adverse events (85 deaths)

Recalls

Facilities

Description

Sentinel, Enteral Feeding Pump, 120VAC Type B

Recalls

Date	Firm	Reason
2021-01-19	Cardinal Health 200, LLC	The potential for air appearing in the enteral feed pumping set tubing during set-up.
2020-09-22	Cardinal Health 200, LLC	The feeding spike sets may leak at the interface of the tube and spike connector.
2020-09-22	Cardinal Health 200, LLC	The feeding spike sets may leak at the interface of the tube and spike connector.
2019-12-26	Cardinal Health Inc.	The feeding spike sets may leak at the interface of the tube and spike connector.
2019-12-26	Cardinal Health Inc.	The feeding spike sets may leak at the interface of the tube and spike connector.
2019-12-26	Cardinal Health Inc.	The feeding spike sets may leak at the interface of the tube and spike connector.
2019-12-26	Cardinal Health Inc.	The feeding spike sets may leak at the interface of the tube and spike connector.
2019-12-26	Cardinal Health Inc.	The feeding spike sets may leak at the interface of the tube and spike connector.
2019-12-26	Cardinal Health Inc.	The feeding spike sets may leak at the interface of the tube and spike connector.
2016-04-01	Medtronic	Kangaroo Connect Feeding Pump Occlusion alarms fail to alarm

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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.