# FDA recall Z-1349-2024

> **Landauer** · Class II · device recall initiated 2024-02-08.

## Product

microStar Reader, Model Numbers:  10015-000 (marketed in EMEA as 100, 102, 110, and 201), 10016-000 (marketed in EMEA as 101), 10036-000, 10044-000, 10055-000, BC30058, and BC30059

## Reason for recall

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.

## Distribution

Worldwide distribution - United States Nationwide and the countries of Argentina, Australia, Brazil, Canada, China, France, India, Japan, Jordan, Malaysia, Mexico, Pakistan, Peru, Philippines, Rep of Korea, Singapore, Sweden, Taiwan, Thailand, Turkey, United Kingdom, Uruguay, Venezuela, Viet Nam.

## Key facts

- **Recall number:** Z-1349-2024
- **Recalling firm:** Landauer
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2024-02-08
- **Report date:** 2024-03-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Glenwood, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1349-2024

## Citation

> AI Analytics. FDA recall Z-1349-2024. Retrieved 2026-06-12 from https://api.ai-analytics.org/recall/Z-1349-2024. Source: US FDA. Licensed CC0.

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