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

Recall Z-0783-2017 — Ultroid Mobile Generator/Battery operated unit including the Ultroid Sterile Disposable Probes

U.S. FDA — Device Enforcement · United States · 2016-10-19 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0783-2017
Date of alert
2016-10-19
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Ultroid Technologies, Inc.
Product category
device
Product type
Devices
Reported risk: Products are not designed, qualified, manufactured, and/or managed under a state of control per internal quality system procedures and external laws, regulations, directives, standards, and/or guidance (such as 21 CFR 820 Quality System Regulation)
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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