Inactivated macrolide and quinolone-resistant Mycoplasma genitalium
Reported: April 27, 2022 Initiated: March 24, 2022 #Z-0954-2022
Product Description
Inactivated macrolide and quinolone-resistant Mycoplasma genitalium
Reason for Recall
QC process was not adequate for the specification range.
Details
- Recalling Firm
- Microbiologics Inc
- Units Affected
- 1 ea
- Distribution
- US Nationwide distribution in the state of TX.
- Location
- Saint Cloud, MN
Frequently Asked Questions
What product was recalled? ▼
Inactivated macrolide and quinolone-resistant Mycoplasma genitalium. Recalled by Microbiologics Inc. Units affected: 1 ea.
Why was this product recalled? ▼
QC process was not adequate for the specification range.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on April 27, 2022. Severity: Moderate. Recall number: Z-0954-2022.
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