Landauer recalls microStar Reader models 10015-000 and others for medical use only. The product is no longer intended for medical applications due to safety concerns.
Permanent discontinuance of the microSTARii medical dosimetry system. Landauer has initiated this action to remove all reference to use of the microStar readers with the nanoDot or any otherbdosimeter for medical applications from the product s user manual and software and to remove microStar readers from customers who use them only for medical applications.
Landauer is recalling microStar Reader devices that were sold for medical use. These products are no longer safe for medical applications and must be discontinued.
The microStar Reader was designed for medical dosimetry but Landauer has discontinued its use in medical applications. The product is no longer safe for medical use due to safety concerns.
Users who purchased microStar Readers intended for medical applications are affected. Medical professionals using these devices for dosimetry are at higher risk.
Check for model numbers 10015-000, 10016-000, 10036-000, 10044-000, 10055-000, BC30058, and BC30059. These models were sold in EMEA regions with specific lot/serial numbers.
Discontinue use of microStar Readers intended for medical applications as they are no longer safe for medical use.
Landauer has discontinued the microStar Reader for medical applications due to safety concerns and no longer intends to use it for medical dosimetry.
Models 10015-000, 10016-000, 10036-000, 10044-000, 10055-000, BC30058, and BC30059 were sold in EMEA regions.
The recall does not specify a return process, but users should stop using medical models as they are no longer safe for medical applications.
We’ve drafted a message you can send Landauer to request your refund or repair — edit it as you like.
Subject: Recall Z-1349-2024 — Landauer Landauer Hello, I own a Landauer that is covered by recall Z-1349-2024 from Landauer. 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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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.
