Leica Microsystems, Inc.: Medical Device Recall in 2018 - (Recall #: Z-0281-2019)

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:

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

Product Classification:

Class II

Date Initiated: September 17, 2018

Date Posted: November 7, 2018

Recall Number: Z-0281-2019

Event ID: 81036

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.

Status: Terminated

Product Quantity: 876 devices (in U.S. and Canada)

Code Information:

Zebra Printer Model TLP3842 - Affected PSU Part Number 808113-001 or P1028888-001 with date codes ranging from 0639XX through 1253XX (YYWWXX, where YY=year and WW=week); Zebra Printer Model GX4301 - Affected PSU Part Number 808101-001 with date codes ranging from 0639XX through 1253XX (YYWWXX, where YY=year and WW=week).

Distribution Pattern:

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

Voluntary or Mandated:

Voluntary: Firm initiated