Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
The Spirit Plus Bed Recalled by Stryker Medical Division of Stryker Corporation Due to The beds with the high rail side rail...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Stryker Medical Division of Stryker Corporation directly.
Affected Products
The Spirit Plus Bed, Model 5600 Spirit Plus /with high rail siderail option
Quantity: 20,030 total
Why Was This Recalled?
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.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Stryker Medical Division of Stryker Corporation
Stryker Medical Division of Stryker Corporation has 79 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report