FDA Medical devices recall ·

Zebra Thermal Barcode Printer GX430t, Model no recall

Recall number
Z-1395-2025
Date
(initiated February 12, 2025)
Company / brand
Remel, Inc
12076 Santa Fe Trail Dr, Lenexa, KS, United States
Category
Medical devices › Class II
Classification
Class II
Status
Ongoing
Units affected
41
Hazard tags
Fire
Initiated by
Voluntary: Firm initiated

Read the official FDA notice ↗

Product

Zebra Thermal Barcode Printer GX430t, Model no. YSW 1000 or YSW 2000, may have been sold as an optional accessory for Sensititre Aris HIQ system YV4000-VZ

Why was it recalled?

Power supply unit for Zebra Printers used with the device can potentially overheat or cause a fire hazard.

What should you do?

FDA enforcement reports do not list a consumer remedy. Check the product codes below against what you have; if it matches, stop using it and follow the instructions in the firm's or FDA's official notice, or contact the company. If you have health concerns, contact your healthcare provider.

Product codes & lot numbers

UDI-DI 05032384545872. Detailed list of affected Zebra printer models: https://www.zebra.com/us/en/power-supply-recall.html Please check the manufacturing label found either on the back or bottom of your printer. If the label lists Zebra Technologies as the manufacturer, please use the validation form on the Zebra website to fully validate if your power supply is affected: https://connect.zebra.com/safeguard

Distribution

Domestic distribution to AL, AZ, CA, FL, GA, IN, KS, KY, MD, MI, NE, NY, OH, PA, TN, TX, WI. International distribution to Canada and the Bahamas.

States: Alabama Arizona California Florida Georgia Indiana Kansas Kentucky Maryland Michigan Nebraska New York Ohio Pennsylvania Tennessee Texas Wisconsin

What does Class II mean?

Class II means use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or the probability of serious harm is remote.

Source: FDA (medical devices), recall Z-1395-2025. Official notice. Republished from public data; RecallFlag is not affiliated with the FDA.