Arjohuntleigh Magog recalls RotoProne Therapy System Model 209800 due to potential delay in emergency patient access from inability to quickly release the proning arm buckle.
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.
Arjohuntleigh Magog is recalling their RotoProne Therapy System Model 209800 because the proning arm buckle may be difficult to unbuckle during emergencies like cardiac arrest, which could delay life-saving assistance.
The proning arm buckle may be difficult to release quickly during emergencies such as cardiac arrest. This delay could prevent timely medical intervention and lead to life-threatening consequences.
Healthcare providers using the RotoProne Therapy System for patient care are most at risk, particularly in emergency situations where quick access is needed.
Check for the RotoProne Therapy System with Model Number 209800. All units are affected regardless of serial number.
Identify the RotoProne Therapy System with Model Number 209800 to confirm if it is affected.
Yes, the proning arm buckle may be difficult to unbuckle during emergencies like cardiac arrest, which could delay life-saving assistance.
Check for the RotoProne Therapy System with Model Number 209800. All units are affected regardless of serial number.
The recall does not specify a remedy, so contact Arjohuntleigh Magog directly for guidance.
We’ve drafted a message you can send Arjohuntleigh Magog to request your refund or repair — edit it as you like.
Subject: Recall Z-0802-2019 — Arjohuntleigh Magog Arjohuntleigh Magog Hello, I own a Arjohuntleigh Magog that is covered by recall Z-0802-2019 from Arjohuntleigh Magog. 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.
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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.
