Recall Z-0954-2022— Microbiologics Inc

Class II · Terminated

Class II FDA medical device recall by Microbiologics Inc, initiated 2022-03-24, terminated 2023-01-09. FDA's recall record names no specific 510(k) clearance for this event. Product: Inactivated macrolide and quinolone-resistant Mycoplasma genitalium. Reason: QC process was not adequate for the specification range..

Recalling firm
Microbiologics Inc
Classification
Class II
Status
Terminated
Initiated
2022-03-24
Terminated
2023-01-09
Firm location
Saint Cloud, MN, United States

Product description

Inactivated macrolide and quinolone-resistant Mycoplasma genitalium

Reason for recall

QC process was not adequate for the specification range.

Data sourced from openFDA. This site is unofficial and independent of the FDA.