Devices

Device Recall Sterile I.V. bag

Model / Serial
FPB NEP, batch # X-003, code 722842.
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Distributed to health care facilities in California, Georgia and Oregon.
Product Description
Gri-bag: A single use, non pyrogenic flexible empty container with an incorporated 0.2 micron filter. It is supplied sterile in sealed peel-pack pouches. It is used to remove particulates in the Gri-fill pharmacy compounding system and as a container in the preparation of drug solutions. || Gri-bag 500 ml.
Manufacturer
Instituto Grifols, S.A.
1 Event
- Recall of Device Recall Sterile I.V. bag

Manufacturer

Instituto Grifols, S.A.

Manufacturer Address
Instituto Grifols, S.A., #2 Can Guasch Street,, Poligono Levante, Parets Del Valles, Barcelona CA Spain 90032-3520
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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