Leica Microsystems, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0019-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2018.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: September 4, 2018

Date Posted: October 10, 2018

Recall Number: Z-0019-2019

Event ID: 80986

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.

Status: Terminated

Product Quantity: 1 unit

Code Information:

Serial Number 102

Distribution Pattern:

Distribution in US state of MO.

Voluntary or Mandated:

Voluntary: Firm initiated