O&M HALYARD, INC.: Medical Device Recall in 2024 - (Recall #: Z-1461-2024)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2024.

Data Source: FDA.

Product Description:

HALYARD SURGICAL HOOD, Universal Size, Blue, 300 count (3 x 100)

Product Classification:

Class III

Date Initiated: February 20, 2024

Date Posted: April 10, 2024

Recall Number: Z-1461-2024

Event ID: 94182

Reason for Recall:

Product was mislabeled as a Surgical Cap at its dispenser level.

Status: Ongoing

Product Quantity: 250 cases (75,000 pieces)

Code Information:

Model No. 69110; UDI-DI: 20680651691105; Lot No. CG22292XXX.

Distribution Pattern:

Worldwide - US Nationwide distribution in the states of AZ, CA, CO, FL, HI, MN, MO, MT, SD, TN, TX, and WA. The country of Canada.

Voluntary or Mandated:

Voluntary: Firm initiated