Reported Feb 14, 2024 · Ongoing
Dual Articulating Headrest, Velcro P/N P141210813, REF BF753
Steris Corporation
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Steris Corporation · 5960 Heisley Rd · Mentor, OH · 44060-1834
Is this the product you have?
Dual Articulating HeadrestVelcro P/N P141210813REF BF753
- Lot codes and dates
- UDI-DI00724995195885, date of manufacture 2023-08-14 thru 2023-10-26
- Amount recalled
- 80
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
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The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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