Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit Recalled by Avanos Medical, Inc. Due to The CORFLO PEG tube may become blocked at...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Avanos Medical, Inc. directly.
Affected Products
CORFLO Percutaneous Endoscopic Gastrostomy (PEG)Kit
Quantity: 1766
Why Was This Recalled?
The CORFLO PEG tube may become blocked at the center of the adapter (occluded) potentially causing a procedure to delayed or aborted.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Avanos Medical, Inc.
Avanos Medical, Inc. has 37 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report