Arjohuntleigh Magog: Medical Device Recall in 2019 - (Recall #: Z-0802-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

ARJOHUNTLEIGH GETINGE GROUP, RotoProne Therapy System, Model Number 209800

Product Classification:

Class II

Date Initiated: December 19, 2018

Date Posted: February 13, 2019

Recall Number: Z-0802-2019

Event ID: 81872

Reason for Recall:

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.

Status: Terminated

Product Quantity: 231 units

Code Information:

All Serial Numbers

Distribution Pattern:

US, Saudi Arabia, and Kuwait

Voluntary or Mandated:

Voluntary: Firm initiated