Stryker recalls Spirit Plus Bed Model 5600 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 Spirit Plus Beds with Model 5600 and high rail siderail option that may not meet safety standards, creating a risk of entrapment. This could affect patients or caregivers using the bed.
The beds may not comply with IEC 60601-2-52/C1:2010 safety standards, which could lead to entrapment. This risk occurs when the siderail mechanism fails to properly secure the bed during use.
Patients and caregivers using the Spirit Plus Bed Model 5600 with high rail siderail option are most at risk. The recall affects specific units with listed serial numbers.
Check if your Spirit Plus Bed has Model 5600 with high rail siderail option. Affected units have specific serial numbers listed in the recall notice.
Identify if your bed has Model 5600 with high rail siderail option and the listed serial numbers.
Reach out to Stryker for guidance on next steps if your bed is affected.
The Spirit Plus Bed Model 5600 with high rail siderail option.
There is a potential risk of entrapment due to non-compliance with IEC 60601-2-52/C1:2010 safety standards.
Check if your bed has Model 5600 with high rail siderail option and the specific serial numbers listed 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-0438-2019 — Stryker Stryker Hello, I own a Stryker that is covered by recall Z-0438-2019 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.
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.
