Avanos Medical, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0371-2020)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

CORFLO* Percutaneous Endoscopic Gastrostomy (PEG) Kit, Labeled as CORFLO* PEG Kit with ENFit Connector. 2 units per case The devices could be branded as Halyard Health.

Product Classification:

Class II

Date Initiated: October 8, 2019

Date Posted: November 20, 2019

Recall Number: Z-0371-2020

Event ID: 84021

Reason for Recall:

The connector piece to the PEG tube does not pass over the guidewire.

Status: Terminated

Product Quantity: 104 cases (208 units) total

Code Information:

Catalog Number: 50-4016E1 (Lot Numbers:0203137961, 0203172166); Catalog Number: 50-4020E1 (Lot Number: 0203069043)

Distribution Pattern:

Distribution to CT, IN, MD, NJ, PA, VA. International distribution to Great Britain.

Voluntary or Mandated:

Voluntary: Firm initiated