# FDA recall Z-0281-2019

> **Leica Microsystems, Inc.** · Class II · device recall initiated 2018-09-17.

## Product

BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301, for use with BOND-III and BOND-MAX instruments

## Reason for recall

The power supply unit for the printer used with the device can potentially overheat or cause a fire hazard because it could contain an improperly-mixed phosphorus compound.

## Distribution

Distribution was nationwide.  There was also government/military distribution.  Foreign distribution was made to Canada.

## Key facts

- **Recall number:** Z-0281-2019
- **Recalling firm:** Leica Microsystems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-09-17
- **Report date:** 2018-11-07
- **Termination date:** 2020-08-21

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0281-2019

## Citation

> AI Analytics. FDA recall Z-0281-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0281-2019. Source: US FDA. Licensed CC0.

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