medical Class II Updated 2022-04-27

Microbiologics Inc recalls Inactivated macrolide and quinolone-resistant Mycoplasma gen

Recalled Product

Inactivated macrolide and quinolone-resistant Mycoplasma genitalium


Hazard / Issue

QC process was not adequate for the specification range.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Catalog HE0069N; Lot HE0069-02-1 UDI: 10845357043990
View official government recall

Looking for safe alternatives?

Browse certified-safe products in this category on Amazon →