Enforcement record

Voluntary Recall disclosure naming 日本マイクロポートCRM株式会社

日本マイクロポートCRM株式会社 (医薬品医療機器等の品質管理等に関する法律)

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

医薬品医療機器等の品質管理等に関する法律Ministry of Health, Labour and WelfareGovernment disclosure31 August 2022

Action type

Voluntary Recall

Law

医薬品医療機器等の品質管理等に関する法律

Authority

Ministry of Health, Labour and Welfare

Action date

31 August 2022

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
Queued for preservation
Captured: Jul 12, 2026, 04:20 PM JST

“Confirmed” means that RegBase matched this record to the cited public disclosure or entity under the stated checks. It does not verify the truth of the disclosure or guarantee the entity’s current status, creditworthiness, or any legal conclusion.

Available sources and saved files are listed in the public documents section below.

Public documents and saved materials

View the original publications, see what was preserved, or download each file below.

Loading materials…

Action summary

Company
日本マイクロポートCRM株式会社Japanese only
Original: 日本マイクロポートCRM株式会社
Governing law
医薬品医療機器等の品質管理等に関する法律
医薬品医療機器等の品質管理等に関する法律
Action type
Voluntary Recall
自主回収
Action date
31 August 2022
Issuing authority
Ministry of Health, Labour and Welfare
厚生労働省
Industry context
医療機器

Violation

Machine-translated summary — verify against original

Provision of information that a voluntary recall (including collection and patient monitoring) of intracardiac implantable pacemaker leads has commenced.

Show original Japanese text

心内膜植込み型ペースメーカリードの自主回収(回収及び患者モニタリング)に着手した旨の情報提供

Compliance context

Context needed

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

Japanese regulatory disclosure under 医薬品医療機器等の品質管理等に関する法律.

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.