Safety Recall: Tenkeido Seiyaku Herbal Medicine Pills for Lower Back Pain and Bruises – Japan CAA

Published by Reclia Safety Desk | June 29, 2026

🚨 Recall Alert

Product: Herbal Medicine Pills for Lower Back Pain and Bruises

Brand: Tenkeido Seiyaku

Hazards: Safety Risk

🇯🇵 Official Japan CAA Recall Notice
Case #00000035347 | View original notice ->

📋 Inscription Fact Summary

Product: Herbal Medicine Pills for Lower Back Pain and Bruises

Brand: Tenkeido Seiyaku

Case Number: #00000035347

Recall Information Record

Case Number: 00000035347
Product: Herbal Medicine Pills for Lower Back Pain and Bruises
Brand: Tenkeido Seiyaku
Hazards: Safety Risk
Source: Japan Consumer Affairs Agency (CAA)

WHAT HAPPENED

Tenkeido Pharmaceutical has announced a recall of its product “Lower Back Specialist, Small Grain Contusion Pills” (腰専門、小粒 打身丸). The recall is triggered by the company’s decision to terminate its manufacturing and marketing authorization business effective December 31, 2026. This cessation means that the company can no longer ensure the quality and safety of products already circulating in the market, posing a potential risk to consumers.

This recall matters because it involves a health product intended for therapeutic use. Without ongoing quality assurance, there is a risk that the product may degrade or become unsafe over time. The Japan Consumer Affairs Agency (CAA) has published this notice under management number 00000035347, referencing the PMDA as a source of further information. Consumers who have purchased this product should take immediate action.

If you have this product, please follow these steps:

  • Stop using the product immediately.
  • Check the product name and packaging to confirm it matches the recalled item.
  • Contact Tenkeido Pharmaceutical or the retailer where you purchased the product for return and refund instructions.
  • Do not dispose of the product until you receive guidance from the company.
  • Monitor the CAA recall information site or PMDA for updates.

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

The manufacturer and marketing authorization holder will cease operations on December 31, 2026 (Reiwa 8). As a result, quality and safety assurance for products already in the market cannot be guaranteed. Recall initiated on June 1, 2026. Reference source: PMDA. Management number: 00000035347.

📅 Timeline: Synchronized Registry Ingestion Engine Active.

❓ Frequently Asked Questions

Q: Which Tenkeido Seiyaku products are affected by this safety list?

A: The recall covers specific batches of Herbal Medicine Pills for Lower Back Pain and Bruises. Refer to official dossier #00000035347 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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