Published by Reclia Safety Desk | June 29, 2026
🚨 Recall Alert
Product: SARS Coronavirus Antigen Kit ImmunoAce SARS-CoV-2 III
Brand: Tauns
Hazards: Safety Risk
Case #00000035321 | View original notice ->
📋 Inscription Fact Summary
Product: SARS Coronavirus Antigen Kit ImmunoAce SARS-CoV-2 III
Brand: Tauns
Case Number: #00000035321
Recall Information Record
Case Number: 00000035321
Product: SARS Coronavirus Antigen Kit ImmunoAce SARS-CoV-2 III
Brand: Tauns
Hazards: Safety Risk
Source: Japan Consumer Affairs Agency (CAA)
WHAT HAPPENED
Japan’s Consumer Affairs Agency has published a recall notice for the Tauns brand SARS Coronavirus Antigen Kit, specifically the ImmunoAce SARS-CoV-2 III product. The recall was initiated on May 27, 2026, and is referenced under management number 00000035321. The notice indicates that the product may exhibit a faint test line caused by a white void in the line area, potentially leading to false positive results.
This issue is significant because false positive results from a COVID-19 antigen test can cause unnecessary anxiety, inappropriate isolation, and potential misallocation of healthcare resources. The recall is being coordinated with the Pharmaceuticals and Medical Devices Agency (PMDA) to ensure proper handling and communication to users and healthcare providers.
Users who have purchased this product should take the following steps:
- Check the product name and packaging to confirm if it matches the recalled item: ImmunoAce SARS-CoV-2 III.
- Discontinue use of any affected kits immediately.
- Contact the manufacturer or distributor using the contact information provided in the recall notice for instructions on return or replacement.
- If you have received a positive result from this kit, consult a healthcare professional for confirmatory testing.
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
Recall initiated on 2026-05-27. Reference source: PMDA. Management number: 00000035321. The issue involves the appearance of a faint test line due to a white void in the line area, which may lead to false positive results.
❓ Frequently Asked Questions
Q: Which Tauns products are affected by this safety list?
A: The recall covers specific batches of SARS Coronavirus Antigen Kit ImmunoAce SARS-CoV-2 III. Refer to official dossier #00000035321 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.