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FDAFDA · Food and drugs·Recall number Z-0282-2014

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

Published November 20, 2013 · Recall initiated: September 30, 2013

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

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).

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Draeger Medical, Inc.
Distributor
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).
Lot
Catalog numbers:MZ00614, MZ01038, MZ02190, MZ02254, and MZ02332
Risk classification
Class II
Area (FDA)
device
Country
United States

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