Avanos Medical, Inc.: Medical Device Recall in 2022 - (Recall #: Z-0846-2022)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2022.

Data Source: FDA.

Product Description:

BALLARD* Multi-Access Port Catheter, Double Swivel Y Elbow, Adult, 14 French; Sterile; Single Use

Product Classification:

Class II

Date Initiated: November 22, 2021

Date Posted: April 6, 2022

Recall Number: Z-0846-2022

Event ID: 89132

Reason for Recall:

Product was distributed with incorrect expiration date.

Status: Terminated

Product Quantity: 6,280 devices (314 cases)

Code Information:

Finished Product Code: 102005202; Alternate Code: 24014-5; Lot No.: 20065842, 30135996, 30135999, 30137463, 30140309, 30138711, and 30141360.

Distribution Pattern:

Worldwide distribution - US Nationwide distribution in the states of Oklahoma and Ohio; The countries of China, France, Germany, Great Britain, Greece, Italy, and Netherlands.

Voluntary or Mandated:

Voluntary: Firm initiated