Devices

Device Recall I.V. Container

Model / Serial
Product Code 2J8003, Lot No. DR16J18096.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Distribution in the US and Canada.
Product Description
Empty IntraVia Container with Non-DEHP Fluid Path, 500mL || Containers are intended for use in the preparation and administration of drug admixtures.
Manufacturer
Baxter Healthcare Corporation
1 Event
- Recall of Device Recall I.V. Container

Manufacturer

Baxter Healthcare Corporation

Manufacturer Address
Baxter Healthcare Corporation, 1 Baxter Pkwy, Deerfield IL 60015-4625
Manufacturer Parent Company (2017)
Baxter International
Source
USFDA

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Disclaimer

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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