Draeger Medical, Inc.: Medical Device Recall in 2015 - (Recall #: Z-2271-2015)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2015.

Data Source: FDA.

Product Description:

Fabius MRI Anesthesia Machine; Fabius MRI is an inhalation anesthesia machine for use in MRI environments in operating, induction and recovery rooms.

Product Classification:

Class II

Date Initiated: June 22, 2015

Date Posted: August 5, 2015

Recall Number: Z-2271-2015

Event ID: 71592

Reason for Recall:

the Fabius MRI or parts of the system were attracted by the magnetic field of the MRI. If the Fabius MRI is positioned too close to the MRI, its parts can be loosened as a result of the magnetic force of the MRI.

Status: Terminated

Product Quantity: 373

Code Information:

Catalog Number(s): 8607300

Distribution Pattern:

US Nationwide Distribution

Voluntary or Mandated:

Voluntary: Firm initiated