Recall archive / FDA device enforcement
Mycoplasma genitalium Control Panel (Inactivated Pellet) — FDA record Z-0784-2022
Reported terminated
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Feb 25, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- Mycoplasma genitalium Control Panel (Inactivated Pellet)
- Reason
- Distributed product did not undergo proper release testing.
- Classification
- Class II
- Recalling firm
- Microbiologics Inc
- Quantity
- 80 units
- Agency-reported status
- Terminated
- Source record identifier
- Z-0784-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | Catalog 8240, Lots: 8240-08, 8240-09, 8240-10, 8240-11, 8240-12, 8240-13, 8240-14, 8240-15, 8240-16 (UDI: 70845357043053) |
Match all identifying details in the current notice. A brand name alone is not enough.
Distribution
Distribution in US: AZ, CT, DC, FL, IL, IN, KS, KY, MA, MD, NC, NH, NJ, NY, PA, TX, UT, WA OUS distribution to Belgium, Finland, France, Germany, Ireland, Sweden, United Kingdom, and Vietnam
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
Dates in the source
- Report date
- Mar 23, 2022
- Recall initiation date
- Feb 25, 2022
- Center classification date
- Mar 14, 2022
- Termination date
- Jan 16, 2024
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.