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AbbVie Inc. recalls AbbVie PEG Kit 20 FR
Recalled December 28, 2016 · FDA recall Z-0786-2017 · AbbVie
Hazard
AbbVie is issuing an urgent field correction notification due to an increased number of reports of disconnections of the AbbVie 20FR PEG tube from the Y-connectors. · FDA Class II
Units
541 units
Sold at
U.S. consignees located throughout the country and Puerto Rico. Foreign Consignees: Worldwide.
Description
AbbVie is issuing an urgent field correction notification due to an increased number of reports of disconnections of the AbbVie 20FR PEG tube from the Y-connectors.
Product
AbbVie PEG Kit 20 FR
Manufacturer(s)
AbbVie Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →