Umano recalls AC-powered adjustable medical beds with built-in electric DC actuators due to potential electrical system failure causing uncontrolled movement. Affected models include specific serial numbers listed in the recall.
There is a potential hazard of uninterrupted motion of the Motorized Wheel System due to the possible failure of a component in the electrical system of the Product.
Umano is recalling AC-powered adjustable medical beds with built-in electric DC actuators because of a potential electrical system failure that could cause uncontrolled movement. This hazard may lead to injury if the bed moves unexpectedly while in use.
The electrical system in these beds may fail, causing the motorized wheel system to move uncontrollably. This could result in injury if the bed shifts unexpectedly while a patient is being moved or positioned.
Healthcare facilities and patients using Umano medical beds with the affected serial numbers. Patients and staff are at risk if the bed moves unexpectedly during use.
Check the serial numbers listed in the recall notice. Affected models include specific serial numbers starting with 20004 and ending with various numbers as detailed in the recall record.
Verify your medical bed's serial number against the list of affected serial numbers provided in the recall notice.
No, but you should check if your bed is affected by the serial numbers listed in the recall. If it is, take action as described.
The recall does not specify a remedy, so contact Umano Medical, Inc. for further instructions.
Check the serial number against the list of affected serial numbers provided in the recall notice.
We’ve drafted a message you can send Umano to request your refund or repair — edit it as you like.
Subject: Recall Z-1136-2022 — Umano Umano Hello, I own a Umano that is covered by recall Z-1136-2022 from Umano. 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.
