Enforcement record

注意喚起 disclosure naming OxyElite Pro

OxyElite Pro (Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices)

This page records one action from a Japanese government disclosure, including the published name, governing law, authority, action details, and official source.

Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical DevicesMinistry of Health, Labour and WelfareGovernment disclosure25 December 2013

Action type

注意喚起

Law

Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices

Authority

Ministry of Health, Labour and Welfare

Action date

25 December 2013

Current page: Enforcement record

This screen focuses on one disclosed action: the published name, governing law, authority, facts, source status, and review evidence.

Source verification

Public-source and preservation status

Publishing authority
Ministry of Health, Labour and Welfare
Official source URL
Recorded by RegBase
Entity match
Not confirmed; shown under the published name
Kiroku preservation
Completed archive verified
Captured: Jul 12, 2026, 03:42 PM JST

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Action summary

Company
OxyElite ProJapanese only
Original: OxyElite Pro
Governing law
Act on Securing Quality, Efficacy and Safety of Pharmaceuticals and Medical Devices
薬機法
Action type
注意喚起
注意喚起
Action date
25 December 2013
Issuing authority
Ministry of Health, Labour and Welfare
厚生労働省
Industry context
サプリメント

Violation

Machine-translated summary — verify against original

The product was obtained through personal importation, and there is no record of OxyElite Pro being imported as a commercial activity in Japan. However, due to the potential for health damage from personal use, a warning notice was again disseminated to prefectural authorities and others as detailed in the attached document.

Show original Japanese text

個人輸入を介して入手したものであり、日本における OxyElite Pro の業としての輸入実績はありませんが、今後も個人使用による健康被害の可能性(注)もあることから、再度、別添のとおり各都道府県等に対し注意喚起について周知を行いました。

Public documents and saved materials

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Compliance context

Context needed

This is a public Japanese regulatory disclosure. The exact legal effect depends on the cited source and regulator.

Health product law covering pharmaceuticals, medical devices, cosmetics, quasi-drugs, labeling, and advertising.

Review the original Japanese source and determine relevance to your counterparty-risk workflow.

This context is an operational aid for review workflows, not a credit opinion or legal conclusion.

About this recordAggregated and translated from public Japanese government disclosures. The English text is for reference only — authoritative content is the linked Japanese source.