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Steris Corporation recalls Dual Articulating Headrest, Velcro P/N P141210813, REF BF753
Recalled February 14, 2024 · FDA recall Z-0984-2024 · Steris
Hazard
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. · FDA Class II
Units
80
Sold at
Worldwide - US Nationwide distribution in the states of AZ, CA, FL, IL, IN, IA, KS, LA, MN, MS, NV, NJ, OH, OK, OR, PA, TN, TX, UT, WA, WI & Puerto Rico, and the countries of Australia, Canada, Mexico & New Zealand.
Description
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.
Product
Dual Articulating Headrest, Velcro P/N P141210813, REF BF753
Manufacturer(s)
Steris Corporation
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →