Avanos Medical, Inc.: Medical Device Recall in 2019 - (Recall #: Z-0370-2020)

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. 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-0370-2020

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: 30-4020 (Lot Numbers:0203145253, 0203081127); Catalog Number: 30-4320 (Lot Numbers: 0002994173, 0202974008, 0202907370, 0203201718, 0203241065)

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated