---
title: "Mycoplasma genitalium Control Panel (Inactivated Pellet) — FDA record Z-0784-2022 | Is It on Recall"
description: "Distributed product did not undergo proper release testing."
url: https://isitonrecall.com/recall/fda-device-z-0784-2022-mycoplasma-genitalium-control-panel-inactivated-pellet/
updated: 2026-10-01
site: "Is It on Recall"
language: en
---

[Recall archive](https://isitonrecall.com/archives/) / 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](https://www.fsis.usda.gov/recalls). [Source coverage and dates](https://isitonrecall.com/sources/).

## 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

[Open the official record](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0784-2022%22)

[What the recall classes mean](https://isitonrecall.com/guides/recall-classes/). 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.

- [Arizona](https://isitonrecall.com/state/arizona/)
- [Connecticut](https://isitonrecall.com/state/connecticut/)
- [District of Columbia](https://isitonrecall.com/state/district-of-columbia/)
- [Florida](https://isitonrecall.com/state/florida/)
- [Illinois](https://isitonrecall.com/state/illinois/)
- [Indiana](https://isitonrecall.com/state/indiana/)
- [Kansas](https://isitonrecall.com/state/kansas/)
- [Kentucky](https://isitonrecall.com/state/kentucky/)
- [Massachusetts](https://isitonrecall.com/state/massachusetts/)
- [Maryland](https://isitonrecall.com/state/maryland/)
- [North Carolina](https://isitonrecall.com/state/north-carolina/)
- [New Hampshire](https://isitonrecall.com/state/new-hampshire/)
- [New Jersey](https://isitonrecall.com/state/new-jersey/)
- [New York](https://isitonrecall.com/state/new-york/)
- [Pennsylvania](https://isitonrecall.com/state/pennsylvania/)
- [Texas](https://isitonrecall.com/state/texas/)
- [Utah](https://isitonrecall.com/state/utah/)
- [Washington](https://isitonrecall.com/state/washington/)

## 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.

## What to do next

Read the official notice for the action that applies to your exact product.

[Read the current instructions](https://api.fda.gov/device/enforcement.json?search=recall_number%3A%22Z-0784-2022%22)

## Related records

[Medical devices records](https://isitonrecall.com/category/medical-devices/) [Microbiologics Inc records](https://isitonrecall.com/brand/microbiologics-inc/)