Devices

Device Recall Zeus

Model / Serial
Product Number 9Z9501G Lot Number: 03022371 exp. 2004-July; 03022392 exp. 2004-July; 03022472 exp 2004-July.
Product Classification
Immunology and Microbiology Devices
Device Class
2
Implanted device?
No
Distribution
The product was distributed to 6 distributors and 24 direct accounts in the United States and Internationally. Canada; Sweden; Costa Rica; Czech; Indonesia.
Product Description
Cytomegalovirus (CMV) IgG ELISA Test System, In-Vitro Diagnostic, manufactured by Zeus Scientific, Inc., Raritan, NJ.
Manufacturer
Zeus Scientific Inc
1 Event
- Recall of Device Recall Zeus

Manufacturer

Zeus Scientific Inc

Manufacturer Address
Zeus Scientific Inc, 200 Evans Way, Branchburg NJ 08876
Source
USFDA

One device with a similar name

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Device Recall ZeusP Lumbar Interbody Device

Model / Serial
Part Number 1-110926B - Lot Number 128945 and Part Number 1-120922B - Lot Number 128946
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
US Distribution to the states of : GA. MI, OK, SC, TX, VA
Product Description
Zeus-P Lumbar Interbody Device
Manufacturer
Amendia, Inc

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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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