Linet recalls Eleganza 5 AC-powered adjustable beds with specific item numbers due to potential side rail malfunction causing improper locking or sticking in upper position.
A component used within the side rail mechanism may malfunction, resulting in the side rail either not locking properly in the upper position or the side rail becoming stuck in the upper position.
Linet is recalling Eleganza 5 adjustable beds that may have side rails that don't lock properly or get stuck in the upper position. This could lead to the bed not supporting a patient safely during medical care.
The side rail mechanism may malfunction, causing the rail to either not lock securely in the upper position or become stuck there. This could compromise patient safety during medical procedures or transfers.
Healthcare facilities using the Eleganza 5 beds with item numbers a) 1GE512055-40, b) 1GE512055-45, c) 1GE512055-85, or d) 1GE512055-95 are most at risk as these beds are used for intensive care patient support.
Check your Eleganza 5 bed's item number against the listed codes: a) 1GE512055-40, b) 1GE512055-45, c) 1GE512055-85, or d) 1GE512055-95. These are specific models sold for intensive care use.
Identify your bed's item number from the list: a) 1GE512055-40, b) 1GE512055-45, c) 1GE512055-85, or d) 1GE512055-95.
Reach out to Linet directly for further instructions on potential fixes or replacements.
Check if your bed's item number matches a) 1GE512055-40, b) 1GE512055-45, c) 1GE512055-85, or d) 1GE512055-95 to see if it's affected.
Contact Linet directly for instructions on potential fixes or replacements.
The recall states that side rails may not lock properly or get stuck, which could compromise patient safety during medical procedures.
We’ve drafted a message you can send Linet to request your refund or repair — edit it as you like.
Subject: Recall Z-0767-2021 — Linet Linet Hello, I own a Linet that is covered by recall Z-0767-2021 from Linet. 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.
