International Medical Devices Database

Manufacturer Address
Sebia, Inc., 400-1705 Corporate Dr., Norcross GA 30093
Source
USFDA
1 Event
- Recall of Device Recall HYDRAGEL 15 Hemoglobin (E)

One device in the database

Device Recall HYDRAGEL 15 Hemoglobin (E)

Model / Serial
Cat. Number 4126, Lot numbers: 22026/01, 14036/01, 12066/02 and 12066/03.
Product Classification
Hematology and Pathology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide (AL, CA, CO, FL, GA, IL, KA, LA, MD, MI, NM, NC, NJ, NY, PA, TX, VA, WI) and Puerto Rico
Product Description
HYDRAGEL 15 Alkaline Hemoglobin (E) kit, in vitro diagnostic, Sebia Parc Technologique Leonard de Vinci, Rue Leonard de Vinci, 91090 Lisses, France

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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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Sebia, Inc.

One device in the database

Device Recall HYDRAGEL 15 Hemoglobin (E)