Class III

Medical Device Recall: HALYARD SURGICAL HOOD, Universal Size, Blue, 300 count (3 x 100)

O&M HALYARD, INC. · February 20, 2024

Reason for Recall

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

Distribution

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.

States Affected

NATIONWIDE

Quantity Affected

250 cases (75,000 pieces)

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1461-2024

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

O&M HALYARD, INC. Medical Device Recall: HALYARD SURGICAL HOOD, Universal Size, Blue, 300 count (3 x 100) | SafeCheck