Mycoplasma genitalium Control Panel — Class II medical device recall Z-0784-2022
Terminated recall by Microbiologics Inc, reported 2022-03-23, distributed in AZ, CT, DC, FL, IL, IN, KS, KY…. Distributed product did not undergo proper release testing.
| Recall number | Z-0784-2022 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Microbiologics Inc, Saint Cloud, MN, United States |
| Recall initiated | 2022-02-25 |
| Classified | 2022-03-14 |
| Reported by FDA | 2022-03-23 |
| Terminated | 2024-01-16 |
| Distributed | AZ, CT, DC, FL, IL, IN, KS, KY, MA, MD, NC, NH, NJ, NY, PA, TX, UT, WA |
| Countries outside the US | BE, DE, FI, FR, GB, IE, SE, VN |
| Quantity | 80 units |
| UPC / GTIN / UDI-DI | 70845357043053 |
| Lot numbers | 8240-08, 8240-09, 8240-10, 8240-11, 8240-12, 8240-13, 8240-14, 8240-15, 8240-16 |
| Model numbers | 8240, 8240-08, 8240-09, 8240-10, 8240-11, 8240-12, 8240-13, 8240-14, 8240-15, 8240-16 |
Product
Mycoplasma genitalium Control Panel (Inactivated Pellet)
Reason for recall
Distributed product did not undergo proper release testing.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0784-2022. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.