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Avanos Medical, Inc. recalls CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit, Labeled as CORFLO* PEG Kit. 2 units per case The devices coul
Recalled November 20, 2019 · FDA recall Z-0370-2020 · Avanos Medical
Hazard
The connector piece to the PEG tube does not pass over the guidewire. · FDA Class II
Units
104 cases (208 units) total
Sold at
Distribution to CT, IN, MD, NJ, PA, VA. International distribution to Great Britain.
Description
The connector piece to the PEG tube does not pass over the guidewire.
Product
CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit, Labeled as CORFLO* PEG Kit. 2 units per case The devices could be branded as Halyard Health.
Manufacturer(s)
Avanos Medical, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →