Microbiologics Mycoplasma Control Panel Recall: Inadequate Testing Risk

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Recalling firmMicrobiologics Inc200 Cooper Ave N, N/A · Saint Cloud, MN 56303-4440

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✎ GovInfoNow plain-language explainer

What happened, in plain English

Microbiologics is recalling specific lots of their Mycoplasma genitalium Control Panel (Inactivated Pellet) because the product did not undergo proper release testing. This could mean the product may not meet safety standards, though the recall does not specify a risk of injury or harm.

Why it’s dangerous

The product did not undergo proper release testing, which means it may not meet safety standards. This could potentially lead to issues with the product's performance or reliability, but the recall does not specify a risk of injury or harm.

Who’s affected

Users of the Mycoplasma genitalium Control Panel (Inactivated Pellet) with the catalog number 8240 and specific lots (8240-08 to 8240-16) are affected. Laboratory or research personnel using this product are most at risk.

How to tell if you have this one

Check if your product has the catalog number 8240 and lots 8240-08 through 8240-16. The unique device identifier (UDI) is 70845357043053.

Brand
Microbiologics
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check Product Details
Verify your product's catalog number and lot numbers to confirm if it is affected.

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Questions people ask

Is there a risk of injury from this product?

The recall does not specify any risk of injury or harm.

What should I do if I have this product?

The recall does not provide a remedy or action steps for affected products.

How can I check if my product is affected?

Check if your product has catalog number 8240 and lots 8240-08 through 8240-16.

Take action

Contact Microbiologics

We’ve drafted a message you can send Microbiologics to request your refund or repair — edit it as you like.

✉️ Open in email

Subject: Recall Z-0784-2022 — Microbiologics Microbiologics

Hello,

I own a Microbiologics that is covered by recall Z-0784-2022 from Microbiologics.

I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this?

Thank you.

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Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

Official source: FDA Recall #Z-0784-2022 (February 25, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0784-2022 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.

Microbiologics Inc recalls Mycoplasma genitalium Control Panel (Inactivated Pellet)

Recall notice