Recall Z-1929-2014— Microgenics Corporation
Class III · Terminated
Class III FDA medical device recall by Microgenics Corporation, initiated 2013-12-02, terminated 2014-07-08. It names one FDA 510(k) clearance: K110616. Product: MAS Omni Immune Controls. Reason: The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni IMMUNE PRO controls; however the package insert was not updated to reflect the change..
- Recalling firm
- Microgenics Corporation
- Classification
- Class III
- Status
- Terminated
- Initiated
- 2013-12-02
- Terminated
- 2014-07-08
- Firm location
- Fremont, CA, United States
510(k) clearances named in this recall
1 on FDA's recordK-numbers as listed on FDA's Recall Enterprise System record for this event (openFDA device/recall k_numbers). The recall may also cover devices cleared under other submissions not named here.
Product description
MAS Omni Immune Controls
Reason for recall
The constituent, Inhibin A, was removed from MAS Omni IMMUNE and MAS Omni IMMUNE PRO controls; however the package insert was not updated to reflect the change.
Data sourced from openFDA. This site is unofficial and independent of the FDA.