Inactivated macrolide and quinolone-resistant recall
Inactivated macrolide and quinolone-resistant Mycoplasma genitalium
Why was Inactivated macrolide and quinolone-resistant recalled?
QC process was not adequate for the specification range.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Catalog HE0069N; Lot HE0069-02-1 UDI: 10845357043990
- Product
- Inactivated macrolide and quinolone-resistant Mycoplasma genitalium
- Recalling firm
- Microbiologics Inc
- Quantity
- 1 ea
- Distribution
- US Nationwide distribution in the state of TX.
- Recall date
- April 27, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)