FDAFDA · Food and drugs·Recall number Z-0954-2022
Inactivated macrolide and quinolone-resistant Mycoplasma genitalium
Published April 27, 2022 · Recall initiated: March 24, 2022
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
QC process was not adequate for the specification range.
What to do
Voluntary: Firm initiated · E-Mail
Recall details
- Manufacturer
- Microbiologics Inc
- Distributor
- US Nationwide distribution in the state of TX.
- Lot
- Catalog HE0069N; Lot HE0069-02-1 UDI: 10845357043990
- Risk classification
- Class II
- Area (FDA)
- device
- Country
- United States
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