Medical Device Recall: Dual Articulating Headrest, Pad Ret P/N P141210805, REF BF754
Steris Corporation · December 12, 2023
Reason for Recall
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.
Distribution
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.
States Affected
NATIONWIDE
Quantity Affected
2
Source: FDA (openFDA Device Enforcement)
Recall number: Z-0983-2024
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.