Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Draeger Movita 603x/DVE 803x Ceiling Supply Unit. It is intended Recalled by Draeger Medical, Inc. Due to Cases were encountered with the Draeger Movita 603x/DVE...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Draeger Medical, Inc. directly.
Affected Products
Draeger Movita 603x/DVE 803x Ceiling Supply Unit. It is intended for use in operating theaters and intensive care
Quantity: 139
Why Was This Recalled?
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).
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Draeger Medical, Inc.
Draeger Medical, Inc. has 78 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report