Reported Apr 27, 2022 · Terminated
Inactivated macrolide and quinolone-resistant Mycoplasma genitalium
Microbiologics Inc.
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: Microbiologics Inc · 200 Cooper Ave N · Saint Cloud, MN · 56303-4440
Is this the product you have?
- Inactivated macrolide and quinolone-resistant Mycoplasma genitalium
- Lot codes and dates
- Catalog HE0069N
- Lot HE0069-02-1 UDI10845357043990
- Amount recalled
- 1 ea
This recall covers 2 products
The agency filed one notice per product. You are reading one of them; the other one is below.
Where it was sold
- Nationwide
- TX
Why it was recalled
QC process was not adequate for the specification range.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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