Low risk — use of or exposure to this product is not likely to cause adverse health consequences.
HALYARD SURGICAL HOOD Recalled by O&M HALYARD, INC. Due to Mislabeling
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact O&M HALYARD, INC. directly.
Affected Products
HALYARD SURGICAL HOOD, Universal Size, Blue, 300 count (3 x 100)
Quantity: 250 cases (75,000 pieces)
Why Was This Recalled?
Product was mislabeled as a Surgical Cap at its dispenser level.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About O&M HALYARD, INC.
O&M HALYARD, INC. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report