Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0281-2019 — BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301, for use with BOND-III and BOND-MAX instruments

U.S. FDA — Device Enforcement · United States · 2018-09-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0281-2019
Date of alert
2018-09-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Leica Microsystems, Inc.
Product category
device
Product type
Devices
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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