Class II — Potential Health Hazard

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...

Date: December 19, 2018
Company: Arjohuntleigh Magog
Status: Terminated
Source: FDA (Device)

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.

Related Recalls

Data sourced from the FDA (Device). Last updated March 26, 2026. View original report