Devices

Device Recall SV900C/D/E (SV900)

Model / Serial
Serial Numbers 010001-188499 Ventilators within the specified serial number range, that are marked with one of the following labels on the inside of the lid of the pneumatic unit are exempted since they have already been fitted with a new type of the pressure transducer. 1. Upgrade EMO 12/02/1; 2. Upgrade SV300 6682-745 SV900 66 82 747.
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Worldwide distribution
Product Description
Maquet Servo Ventilator SV900C/D/E (SV900) || Siemens-Elema AB, Solna, Sweden
Manufacturer
MAQUET Inc.
1 Event
- Recall of Device Recall SV900C/D/E (SV900)

Manufacturer

MAQUET Inc.

Manufacturer Address
MAQUET Inc., 45 Barbour Pond Drive, Wayne NJ 07470
Manufacturer Parent Company (2017)
Getinge AB
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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