Class II — Microbiologics Inc
| Recalling firm | Microbiologics, Inc. |
|---|---|
| Registered facility | Microbiologics, Inc. (the firm's only registered facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | The QC process was not adequate for the specification range. |
| Product | Inactivated macrolide-resistant Mycoplasma genitalium |
| Quantity | 2 ea |
| Distribution | US Nationwide distribution in the states of NV and VT. |
| Initiated | 2022-03-22 |
| Classified | 2022-04-19 |
| Terminated | 2023-01-09 |
| Recall number | Z-0955-2022 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — Microbiologics Inc (Z-0955-2022).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/89887/
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