Safety Recall: Dord Pharmaceutical Dordmin 3000 and 6 Other Products – Japan CAA

Published by Reclia Safety Desk | August 31, 2026

🚨 Recall Alert

Product: Dordmin 3000 and 6 Other Products

Brand: Dord Pharmaceutical

Hazards: Safety Risk

🇯🇵 Official Japan CAA Recall Notice
Case #00000035713 | View original notice ->

📋 Inscription Fact Summary

Product: Dordmin 3000 and 6 Other Products

Brand: Dord Pharmaceutical

Case Number: #00000035713

Recall Information Record

Case Number: 00000035713
Product: Dordmin 3000 and 6 Other Products
Brand: Dord Pharmaceutical
Hazards: Safety Risk
Source: Japan Consumer Affairs Agency (CAA)

WHAT HAPPENED

Dord Pharmaceutical has announced a recall of Dordmin 3000 and six other products. The products were shipped without the required manufacturing records and test records being created. This raises regulatory compliance concerns because the quality and safety of the affected items cannot be fully verified through normal documentation procedures. The recall was initiated after this issue was identified, and the official response began on August 20, 2026. The notice references PMDA as the related information source, and the management number for this case is 00000035713. The absence of proper records means that consumers may be using products whose manufacturing and quality testing history is undocumented. While the notice does not specify a particular defect, the lack of traceability and verification is a serious issue under Japanese recall regulations. Consumers should confirm whether they have any of the affected products and stop using them until more information is available.

  • Check the recalled product names and packaging to see whether your product is one of the affected items.
  • Stop using the product immediately if it matches the recalled range.
  • Contact Dord Pharmaceutical or consult the official Consumer Affairs Agency and PMDA recall information pages for further instructions.
  • Follow the company’s return or disposal procedures as announced.

AFFECTED BATCHES & TARGET SPECIFICS

– **Target Model / Type:** N/A
– **JAN Barcode:** N/A
– **Affected Serial / Lot Numbers:** N/A
– **Total Units Affected:** N/A

ADDITIONAL REGULATORY NOTES

This recall was initiated because the affected products were shipped without manufacturing records and test records being created. The recall response began on August 20, 2026. Reference information is available from PMDA. Management number: 00000035713.

📅 Timeline: Synchronized Registry Ingestion Engine Active.

❓ Frequently Asked Questions

Q: Which Dord Pharmaceutical products are affected by this safety list?

A: The recall covers specific batches of Dordmin 3000 and 6 Other Products. Refer to official dossier #00000035713 for verified metrics.

Q: What physical hazard does this present?

A: Identified hazard vectors include: Safety Risk.

Q: What actions should affected users take?

A: Stop using the unit immediately. Follow official safety guidelines: View original CAA notice.

Disclaimer: Information on this page is summarized from official Japan Consumer Affairs Agency (CAA) recall notices.

Consumers should refer to the original Japan CAA notice for complete details.

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