Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Arjo medical beds Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o. Due to Unintended movement of bed wheels
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 ARJOHUNTLEIGH POLSKA Sp. z.o.o. directly.
Affected Products
Arjo medical beds, Models Enterprise 5000X, Enterprise 8000X, Enterprise 9000X and Citadel, assembled with IndiGo Drive Assistance module and retrofitted with IndiGo Drive Assistance modules
Quantity: 83 units
Why Was This Recalled?
Unintended movement of bed wheels
Where Was This Sold?
This product was distributed to 7 states: CA, IL, NV, NY, PA, SD, TN
About ARJOHUNTLEIGH POLSKA Sp. z.o.o.
ARJOHUNTLEIGH POLSKA Sp. z.o.o. has 9 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report