Devices

Device Recall IVF Pasteur Pipettes

Model / Serial
160306022 EXP 1/22/2010 160306046 EXP 2/15/2010 160306065 EXP 3/6/2010
Product Classification
Obstetrical and Gynecological Devices
Device Class
2
Implanted device?
No
Distribution
The recalled product was distributed to 2 direct accounts in IL and to 6 international distributors in United Kingdom, Greece, Australia, United Arab Emirates, the Netherlands, and Israel.
Product Description
IVF Pasteur Pipettes, glass, cotton plugged, length 9", in boxes of 90 consisting of 30 nylon tube packages of 3 pipettes each. Item # PP-9-90PL. Boxes are labeled in part ***Humagen Fertility Diagnostics, Inc. 2400 Hunter's Way Charlottesville, VA 22911***
Manufacturer
Humagen Fertility Diagnostics, Inc.
1 Event
- Recall of Device Recall IVF Pasteur Pipettes

Manufacturer

Humagen Fertility Diagnostics, Inc.

Manufacturer Address
Humagen Fertility Diagnostics, Inc., 2400 Hunters Way, Charlottesville VA 22911-7930
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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