Steris recalls Dual Articulating Headrest models from August 14 to October 26, 2023, due to potential failure to lock during patient procedures, risking injury or delays.
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 is recalling certain Dual Articulating Headrests that may not stay in place or lock during patient procedures, which could cause patient injury or procedural delays. This recall affects medical devices used in healthcare settings.
The headrest may not stay securely in place or fail to lock during critical patient procedures. This could lead to the headrest moving unexpectedly, potentially causing injury to the patient or delaying necessary medical steps.
Healthcare providers using the recalled headrests in medical procedures are most at risk. Patients receiving care during procedures with the faulty headrest could also be affected.
Check for the Velcro part number P141210813 and reference number BF753 on the headrest. The product was manufactured between August 14 and October 26, 2023.
Ensure the headrest locks securely during procedures; if it moves unexpectedly, stop use immediately.
The recall indicates a risk of failure during procedures, so it is not safe to use without checking the recall status.
Look for Velcro part number P141210813 and reference number BF753, manufactured between August 14 and October 26, 2023.
The recall does not specify a remedy, so contact Steris Corporation for guidance on safe use or alternatives.
We’ve drafted a message you can send Steris to request your refund or repair — edit it as you like.
Subject: Recall Z-0984-2024 — Steris Steris Hello, I own a Steris that is covered by recall Z-0984-2024 from Steris. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
