The CORFLO Safety PEG Kit With ENfit Connector (model/catalogue 50-5320) with lot/serial numbers 30365231 and 30371022 is affected. It was recalled because of quality issues related to sterility assurance for certain lidocaine hydrochloride injection products packaged within the kit. Contact the manufacturer, Avanos Medical, Inc., for additional information.
What's being recalled
Companies: Avanos Medical, Inc., 5405 Windward Parkway, Alpharetta, Georgia, United States, 30004-3894.
How to identify it
Affected products: CORFLO* Safety PEG Kit With ENfit® Connector; Lot or serial number: 30365231; Model or catalogue number: 50-5320
Affected products: CORFLO* Safety PEG Kit With ENfit® Connector; Lot or serial number: 30371022; Model or catalogue number: 50-5320
The hazard
This recall is initiated due to quality issues related to sterility assurance to certain lidocaine hydrochloride injection products. This product is packaged within the CORFLO* Safety PEG Kit With ENfit® Connector.
What to do
Contact the manufacturer if you require additional information.
The official notice
This page is a summary of the notice published by Health Canada, collected from Health Canada, CFIA and Transport Canada. Check the original before you act on it.
Read the official notice (opens in a new tab)