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Panakeia Pharmaceuticals “Shin Curief Gastrointestinal Medicine Plus” - Recall

Official notice

28 Oct 2026

Last checked

28 Oct 2026

RecallScope risk estimate:MediumCAA Japan

An official CAA Japan notice concerns Panakeia Pharmaceuticals “Shin Curief Gastrointestinal Medicine Plus” - Recall. Lots identified with sodium copper chlorophyllin, an active ingredient, below the approved content specification. Reason for recall: Stability monitoring identified a lot with sodium copper chlorophyllin, an active ingredient, below the approved content specification. Examination of retained samples from all lots of this product shipped to the market identified additional lots similarly below the approved specification. The company is therefore voluntarily recalling those lots and lots that may fall below the approved specification within their shelf life. Specific potential health effects: Although the content of this active ingredient may be below the approved specification, all other active ingredients meet the approved specifications. The company considers that there is no risk of an impact on safety or serious health effects resulting from this issue. No reports of health effects or other problems attributable to this issue have been received to date. Published 2026-10-28.

What to do now

The company has identified the shipment recipients and will notify them of the recall in writing and promptly collect the products.

Recall number

2-13012

Official notice

2026-10-28

The hazard

Lots identified with sodium copper chlorophyllin, an active ingredient, below the approved content specification. Reason for recall: Stability monitoring identified a lot with sodium copper chlorophyllin, an active ingredient, below the approved content specification. Examination of retained samples from all lots of this product shipped to the market identified additional lots similarly below the approved specification. The company is therefore voluntarily recalling those lots and lots that may fall below the approved specification within their shelf life. Specific potential health effects: Although the content of this active ingredient may be below the approved specification, all other active ingredients meet the approved specifications. The company considers that there is no risk of an impact on safety or serious health effects resulting from this issue. No reports of health effects or other problems attributable to this issue have been received to date.

How to check if you're affected

Compare the product name and identifiers below with the item you own. Check the official notice for the affected products and next steps.

Lots

H063L 18包 17

Recall Numbers

2-13012

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Affected products

Product 1

新クリエフ胃腸薬プラス

Hazard

Lots identified with sodium copper chlorophyllin, an active ingredient, below the approved content specification. Reason for recall: Stability monitoring identified a lot with sodium copper chlorophyllin, an active ingredient, below the approved content specification. Examination of retained samples from all lots of this product shipped to the market identified additional lots similarly below the approved specification. The company is therefore voluntarily recalling those lots and lots that may fall below the approved specification within their shelf life. Specific potential health effects: Although the content of this active ingredient may be below the approved specification, all other active ingredients meet the approved specifications. The company considers that there is no risk of an impact on safety or serious health effects resulting from this issue. No reports of health effects or other problems attributable to this issue have been received to date.

Where it was sold

Retailer information is not currently available in RecallScope. Check the official notice for distribution details.

Location 1

JP · Japan

Affected area 1

JP · Japan

Company & contacts

Brand

パナケイア製薬

Manufacturer

株式会社パナケイア製薬

Phone

0766-36-1118

Brand: パナケイア製薬. Contact: 株式会社パナケイア製薬. Phone 0766-36-1118.

Source & status

Source

Tier

official

Category

HEALTH

Official classification

PMDA Class II — 回収

Recall details

Recall number

2-13012

Event id

CAA-00000036054

Source tier

official

Documents, notices & source

See the official notice and source documents for full details.

View full official notice
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