Draeger Movita 603x/DVE 803x Ceiling Supply Unit — Class II medical device recall Z-0282-2014
Terminated recall by Draeger Medical, Inc., reported 2013-11-20, distributed nationwide. Cases were encountered with the Draeger Movita 603x/DVE 803x Ceiling Supply Units where the drive screw in the
| Recall number | Z-0282-2014 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Draeger Medical, Inc., Telford, PA, United States |
| Recall initiated | 2013-09-30 |
| Classified | 2013-11-14 |
| Reported by FDA | 2013-11-20 |
| Terminated | 2014-09-03 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 139 |
| Model numbers | MZ00614, MZ01038, MZ02190, MZ02254, MZ02332 |
Product
Draeger Movita 603x/DVE 803x Ceiling Supply Unit. It is intended for use in operating theaters and intensive care
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).
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0282-2014. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.