BOND Slide Labeler Zebra Printer Model TLP3842 and Model GX4301 — Class II medical device recall Z-0281-2019
Terminated recall by Leica Microsystems, Inc., reported 2018-11-07, distributed nationwide. The power supply unit for the printer used with the device can potentially overheat or cause a fire hazard bec
| Recall number | Z-0281-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Leica Microsystems, Inc., Buffalo Grove, IL, United States |
| Recall initiated | 2018-09-17 |
| Classified | 2018-10-26 |
| Reported by FDA | 2018-11-07 |
| Terminated | 2020-08-21 |
| Distributed | Nationwide (US) |
| Countries outside the US | CA |
| Quantity | 876 devices |
| Reason classes | device malfunction |
| Model numbers | 808101-001, 808113-001, GX4301, P1028888-001, TLP3842 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0281-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.