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Avanos Medical, Inc. recalls Avanos Cortrak 2 Enteral Access System (EAS)
Recalled May 25, 2022 · FDA recall Z-1032-2022 · Avanos Medical
Hazard
Product labeling is being modified. STOP using the Anonymous Account Mode feature of the CORTRAK 2 device immediately. CONFIRM placement of the NG/NI tube per institution protocol. · FDA Class I
Units
721 devices
Sold at
Worldwide Distribution. US Nationwide, Australia, Austria, Canada, Germany, Ireland, Kuwait, New Zealand, India, Japan, Malaysia, Netherlands, Panama, Singapore, Switzerland, and United Kingdom.
Description
Product labeling is being modified. STOP using the Anonymous Account Mode feature of the CORTRAK 2 device immediately. CONFIRM placement of the NG/NI tube per institution protocol.
Product
Avanos Cortrak 2 Enteral Access System (EAS)
Manufacturer(s)
Avanos Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →