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Stop using now Medical device recall · FDA · Published January 24, 2020

bioMerieux PREVI Isola Printer PSUs: Overheating Fire Hazard

bioMerieux recalls PREVI Isola printer power supply units (PSUs) used in Zebra LP2824 printers that may overheat and cause fire. Affected units have specific date codes and instrument serial numbers.

🇺🇸 FDA recall #Z-1793-2020Medical devicebioMerieux ›
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Recalling firmbioMerieux, Inc.100 Rodolphe St · Durham, NC 27712-9402
✎ GovInfoNow plain-language explainer

What happened, in plain English

bioMerieux is recalling power supply units for PREVI Isola instruments and Zebra LP2824 printers that could overheat and cause fire. If you own these PSUs with the listed date codes or serial numbers, stop using them immediately. Read more at govinfonow.com/recall/65953-biomerieux-previ-isola-printer-psus-overheating-fire-hazard.

Source Summary by GovInfoNow · govinfonow.com/recall/65953-biomerieux-previ-isola-printer-psus-overheating-fire-hazard · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1793-2020

Cite this page

“bioMerieux PREVI Isola Printer PSUs: Overheating Fire Hazard.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/65953-biomerieux-previ-isola-printer-psus-overheating-fire-hazard. Based on FDA recall #Z-1793-2020 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1793-2020%22&limit=1).

Why it’s dangerous

The power supply units (PSUs) in the PREVI Isola instruments can overheat and potentially cause a fire. This hazard occurs when the PSU is used in the Zebra LP2824 Plus printer, which may lead to serious injury or property damage if not addressed.

Who’s affected

Users of PREVI Isola instruments with specific power supply units (PSUs) used in Zebra LP2824 printers. Those with the listed date codes or instrument serial numbers are most at risk.

How to tell if you have this one

Check the PSU's date code (0639XX through 1253XX in YYWWXX format) and instrument serial number listed in the recall notice. The affected PSUs are used in Zebra LP2824 Plus printers.

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

What to do — step by step

  1. Stop Using PSU Now

    Immediately stop using the power supply unit if it has a date code of 0639XX through 1253XX (YYWWXX format) or matches the listed instrument serial numbers.

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

Alaska: yesAKMaine: yesMEVermont: yesVTNew Hampshire: yesNHWashington: yesWAIdaho: yesIDMontana: yesMTNorth Dakota: yesNDMinnesota: yesMNIllinois: yesILWisconsin: yesWIMichigan: yesMINew York: yesNYRhode Island: yesRIMassachusetts: yesMAOregon: yesORNevada: yesNVWyoming: yesWYSouth Dakota: yesSDIowa: yesIAIndiana: yesINOhio: yesOHPennsylvania: yesPANew Jersey: yesNJConnecticut: yesCTCalifornia: yesCAUtah: yesUTColorado: yesCONebraska: yesNEMissouri: yesMOKentucky: yesKYWest Virginia: yesWVVirginia: yesVAMaryland: yesMDDelaware: yesDEArizona: yesAZNew Mexico: yesNMKansas: yesKSArkansas: yesARTennessee: yesTNNorth Carolina: yesNCSouth Carolina: yesSCDistrict of Columbia: yesDCOklahoma: yesOKLouisiana: yesLAMississippi: yesMSAlabama: yesALGeorgia: yesGAHawaii: yesHITexas: yesTXFlorida: yesFL

FDA distribution: “Worldwide distribution. US nationwide including AU, BE, CH, DE, ES, FR, IT, HK/CN; MX, NL, RU, SE/FI, ZA.” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA terminated this recall 3 years after the firm started it.

1. Firm started the recall: Jan 24, 202012. FDA classified it Class II: Apr 23, 202023. Published in FDA’s Enforcement Report: Apr 29, 202034. FDA terminated the recall: Jan 11, 2023420202023
  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.

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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-1793-2020 (January 24, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1793-2020 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