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

Class I - Dangerous
🏥 Medical Devices Recalled: September 30, 2013 Draeger Medical Infusion Pumps Nationwide

What Should You Do?

  1. Check if you have this product:
    Catalog numbers:MZ00614, MZ01038, MZ02190, MZ02254, and MZ02332
  2. Do not eat it: Even if it looks and smells fine, do not consume this product.
  3. Throw it away or return it: You can return the product to the store for a full refund.
  4. Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
  5. Report problems: Report any issues to the FDA's Safety Reporting Portal.

⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.

Recall Details

Company:
Draeger Medical, Inc.
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).
Classification:
Class I - Dangerous

Dangerous or defective products that predictably could cause serious health problems or death.

Status:
terminated

Product Information

Full Description:

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

Product Codes/Lot Numbers:

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

Official Source

Always verify recall information with the official FDA source:

View on FDA.gov

FDA Recall Number: Z-0282-2014

Related Recalls