# FDA recall Z-0019-2019

> **Leica Microsystems, Inc.** · Class II · device recall initiated 2018-09-04.

## Product

Leica HistoCore SPECTRA CV Coverslipper, used in preparation of histological and cytological tissue samples for microscopic analysis for medical diagnostics.

## Reason for recall

Product was assembled with an isolating fiberglass hose within the oven in the wrong position. This results in improper shielding from potential electrical shock.

## Distribution

Distribution in US state of MO.

## Key facts

- **Recall number:** Z-0019-2019
- **Recalling firm:** Leica Microsystems, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-09-04
- **Report date:** 2018-10-10
- **Termination date:** 2020-07-10

- **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-0019-2019

## Citation

> AI Analytics. FDA recall Z-0019-2019. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-0019-2019. Source: US FDA. Licensed CC0.

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