Avanos Medical, Inc. recalls CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit

Recalled May 6, 2020 · FDA recall Z-1822-2020 · Avanos Medical

Hazard

The CORFLO PEG tube may become blocked at the center of the adapter (occluded) potentially causing a procedure to delayed or aborted. · FDA Class II

Units

1766

Sold at

Worldwide and US Nationwide Distribution: AZ, CA, CT, FL, GA, IA, ID, IL, LA, MO, MN, MD, NY, NM, NV, NJ, OR, OK, OH, RI, TN, TX, WA, WI, ***Foreign: Distributed to Australia, Belgium, Canada, France, Germany, Ireland, Italy, Netherlands, Romania, United Arab Emirates, United Kingdom

Description

The CORFLO PEG tube may become blocked at the center of the adapter (occluded) potentially causing a procedure to delayed or aborted.

Product

CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit

Manufacturer(s)

Avanos Medical, Inc.

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →