Draeger Medical, Inc.: Medical Device Recall in 2013 - (Recall #: Z-0282-2014)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2013.

Data Source: FDA.

Product Description:

Draeger Movita 603x/DVE 803x Ceiling Supply Unit. It is intended for use in operating theaters and intensive care

Product Classification:

Class II

Date Initiated: September 30, 2013

Date Posted: November 20, 2013

Recall Number: Z-0282-2014

Event ID: 66537

Reason for Recall:

Cases were encountered with the Draeger Movita 603x/DVE 803x Ceiling Supply Units where the drive screw in the motor unit broke and the lift arm fell down approximately 60 cm (23.6 inches).

Status: Terminated

Product Quantity: 139

Code Information:

Catalog numbers:MZ00614, MZ01038, MZ02190, MZ02254, and MZ02332

Distribution Pattern:

Worldwide distribution: US (Nationwide)and in the country of Canada. (note: the ceiling supply units are not classified as a medical device by Health Canada).

Voluntary or Mandated:

Voluntary: Firm initiated