Inactivated macrolide-resistant Mycoplasma genitalium
Reported: April 27, 2022 Initiated: March 22, 2022 #Z-0955-2022
Product Description
Inactivated macrolide-resistant Mycoplasma genitalium
Reason for Recall
The QC process was not adequate for the specification range.
Details
- Recalling Firm
- Microbiologics Inc
- Units Affected
- 2 ea
- Distribution
- US Nationwide distribution in the states of NV and VT.
- Location
- Saint Cloud, MN
Frequently Asked Questions
What product was recalled? ▼
Inactivated macrolide-resistant Mycoplasma genitalium. Recalled by Microbiologics Inc. Units affected: 2 ea.
Why was this product recalled? ▼
The 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-0955-2022.
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