Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Dual Articulating Headrest Recalled by Steris Corporation Due to Dual-articulating head rest may not stay in place...
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 Steris Corporation directly.
Affected Products
Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754
Quantity: 2
Why Was This Recalled?
Dual-articulating head rest may not stay in place or may fail to lock into position during a patient procedure which could result in an injury to the patient or a procedural delay.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Steris Corporation
Steris Corporation has 109 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report