Stryker recalls Spirit Select Bed Model 5700 Spirit Plus with high rail siderail option due to potential entrapment risk. Affected units have specific serial numbers listed in the recall notice.
The beds with the high rail side rail option may not be complaint with IEC 60601-2-52/C1:2010. There is a potential risk of entrapment.
Stryker is recalling certain Spirit Select Beds (Model 5700 Spirit Plus with high rail siderail option) because they may not meet safety standards and could cause entrapment. This is a safety issue that requires attention to prevent injury.
The bed's high rail siderail option may not comply with safety standards (IEC 60601-2-52/C1:2010), creating a risk of entrapment. This could happen if the side rail mechanism malfunctions or is improperly adjusted.
Healthcare facilities using the Spirit Select Bed Model 5700 Spirit Plus with high rail siderail option are most at risk. Patients or staff could be entangled if the bed's side rail mechanism fails.
Check if your bed has the Spirit Select Bed Model 5700 Spirit Plus with high rail siderail option. Affected units have specific serial numbers listed in the recall notice (see full list in the official notice).
Verify if your bed is the Spirit Select Bed Model 5700 Spirit Plus with high rail siderail option by checking the serial number against the list provided in the recall notice.
Reach out to Stryker directly for guidance on next steps and to confirm if your bed is affected.
The bed's high rail siderail option may not meet safety standards (IEC 60601-2-52/C1:2010), creating a risk of entrapment.
Check the serial number against the list of affected units provided in the recall notice.
We’ve drafted a message you can send Stryker to request your refund or repair — edit it as you like.
Subject: Recall Z-0439-2019 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0439-2019 from Stryker. 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.
