Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
ARJOHUNTLEIGH GETINGE GROUP Recalled by Arjohuntleigh Magog Due to Inability or difficulty in unbuckling/releasing the proning arm...
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 Magog directly.
Affected Products
ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800
Quantity: 231 units
Why Was This Recalled?
Inability or difficulty in unbuckling/releasing the proning arm buckle might delay patient access in an emergency situation such as cardiac arrest. This, in turn, could contribute to a life-threatening event.
Where Was This Sold?
US, Saudi Arabia, and Kuwait
About Arjohuntleigh Magog
Arjohuntleigh Magog has 3 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report