Steris Corporation Dual Articulating Headrest, Velcro P/N P141210813, REF BF753 Recall
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Dual Articulating Headrest, Velcro P/N P141210813, REF BF753
Brand
Steris Corporation
Lot Codes / Batch Numbers
UDI-DI: 00724995195885, date of manufacture 2023-08-14 thru 2023-10-26.
Products Sold
UDI-DI: 00724995195885, date of manufacture 2023-08-14 thru 2023-10-26.
Steris Corporation is recalling Dual Articulating Headrest, Velcro P/N P141210813, REF BF753 due to 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 . Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
An Urgent Medical Device Recall notice dated December 5, 2023 was issued to distributors and customers via FedEx explaining the removal of specific affected product . The notice explains the labeled date of manufacture must fall between August 14, 2023 and October 26, 2023 the recall notice must have been received directly from STERIS. The 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. STERIS Service Technician will work with your facility to schedule a time to hand-deliver replacement head rest(s) and pick up your affected head rest(s). It is recommended all head rests impacted by this recall be immediately removed from service until it can be replaced. If you have further distributed this product, please identify all locations, notify them of this recall, and coordinate the collection of all affected head rest(s).
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026