Skip to content
Lower risk Medical device recall · FDA · Published March 3, 2022

Microbiologics Pneumonia Control Panel Recall: Shorter Shelf Life Than Stated

Microbiologics recalls Pneumonia (33 Targets) Control Panel due to shorter shelf life than advertised. This quality control material expires in 6 months instead of 18 months.

🇺🇸 FDA recall #Z-0844-2022Medical deviceMicrobiologics ›
Take action

Contact the company

Recalling firmMicrobiologics Inc200 Cooper Ave N · Saint Cloud, MN 56303-4440
✎ GovInfoNow plain-language explainer

What happened, in plain English

Microbiologics recalls a specific pneumonia testing control panel because it has a shorter shelf life than promised—only 6 months instead of 18 months. This means the product could become outdated or ineffective before its intended use period ends. Read more at govinfonow.com/recall/60996-microbiologics-pneumonia-control-panel-recall-shorter-shelf-life-than-stated.

Source Summary by GovInfoNow · govinfonow.com/recall/60996-microbiologics-pneumonia-control-panel-recall-shorter-shelf-life-than-stated · Updated August 19, 2026 · FDA enforcement record: FDA #Z-0844-2022

Cite this page

“Microbiologics Pneumonia Control Panel Recall: Shorter Shelf Life Than Stated.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/60996-microbiologics-pneumonia-control-panel-recall-shorter-shelf-life-than-stated. Based on FDA recall #Z-0844-2022 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0844-2022%22&limit=1).

Why it’s dangerous

The control panel expires after 6 months instead of 18 months. If used after this period, it may not provide accurate test results, potentially leading to incorrect diagnoses.

Who’s affected

Laboratories or healthcare facilities using this control panel for pneumonia testing. Those most at risk are users who rely on the panel for accurate test results before its expiration date.

How to tell if you have this one

Check for the catalog number 8244 on the panel. The expiration date on the label should be 07/31/2022 for the first panel and 08/31/2022 for the second panel.

  • Brand
    Microbiologics
  • Category
    Medical device
Based on the official FDA remedy

What to do — step by step

  1. Check Expiration Date

    Verify the expiration date on the panel label to confirm it matches the stated dates (07/31/2022 or 08/31/2022).

Where it went and when

Where it was distributed

Distributed in 8 states.

Alaska: not listedAKMaine: not listedMEVermont: not listedVTNew Hampshire: not listedNHWashington: not listedWAIdaho: not listedIDMontana: yesMTNorth Dakota: not listedNDMinnesota: not listedMNIllinois: yesILWisconsin: yesWIMichigan: not listedMINew York: not listedNYRhode Island: not listedRIMassachusetts: not listedMAOregon: not listedORNevada: not listedNVWyoming: not listedWYSouth Dakota: not listedSDIowa: not listedIAIndiana: not listedINOhio: not listedOHPennsylvania: yesPANew Jersey: not listedNJConnecticut: not listedCTCalifornia: not listedCAUtah: not listedUTColorado: not listedCONebraska: not listedNEMissouri: not listedMOKentucky: not listedKYWest Virginia: not listedWVVirginia: not listedVAMaryland: not listedMDDelaware: not listedDEArizona: not listedAZNew Mexico: not listedNMKansas: not listedKSArkansas: not listedARTennessee: yesTNNorth Carolina: not listedNCSouth Carolina: not listedSCDistrict of Columbia: not listedDCOklahoma: not listedOKLouisiana: not listedLAMississippi: not listedMSAlabama: yesALGeorgia: yesGAHawaii: not listedHITexas: yesTXFlorida: not listedFL

FDA distribution: “US distribution to Alabama, Georgia, Illinois, Montana, Pennsylvania, Tennessee, Texas, and Wisconsin” States read from FDA’s own wording; “not listed” means the notice does not name it.

States: Alabama, Georgia, Illinois, Montana, Pennsylvania, Tennessee, Texas, Wisconsin.

Recall timeline

FDA terminated this recall 22 months after the firm started it.

1. Firm started the recall: Mar 3, 202212. FDA classified it Class II: Mar 31, 202223. Published in FDA’s Enforcement Report: Apr 6, 202234. FDA terminated the recall: Jan 16, 2024420222024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

Similar recalls

Latest medical device recalls

Keep exploring

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-0844-2022 (March 3, 2022) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0844-2022 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.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA