Steris recalls certain Dual Articulating Headrest models (P/N P141210805, REF BF754) 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 specific Dual Articulating Headrest models that may not stay securely 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 in place or lock properly during patient procedures, potentially causing injury to the patient or delaying medical treatment. This happens because the locking mechanism could fail under normal use conditions.
Healthcare providers using the recalled headrests in medical procedures are most at risk. The recall applies to headrests sold between August 14 and October 26, 2023.
Check for the product number P141210805 and reference number BF754 on the headrest. The recall covers units manufactured from August 14 to October 26, 2023.
Look for the product number P141210805 and reference number BF754 on the headrest.
The recall does not provide a specific recall number; it references the product model and manufacturing dates.
The headrests were manufactured from August 14 to October 26, 2023.
The recall does not specify a fix; the remedy is null in the official record.
We’ve drafted a message you can send Steris to request your refund or repair — edit it as you like.
Subject: Recall Z-0983-2024 — Steris Steris Hello, I own a Steris that is covered by recall Z-0983-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
