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日本製薬工業株式会社 "Medicine: Panaberin F" - Recall
Official notice
11 Mar 2003
Last checked
28 Oct 2026
An official CAA Japan notice concerns 日本製薬工業株式会社 "Medicine: Panaberin F" - Recall. The manufacturing method for the active pharmaceutical ingredient (Scopolia extract powder) manufactured by アルプス薬品工業株式会社 and used in this product differed from the approved method. (A different extraction solvent was used.) [Specific potential health harm] We have confirmed that this product meets all approved specifications. No adverse health effects associated with this product have been reported to date. Published 2003-03-11.
What to do now
Consumer instructions are not currently available in RecallScope. Check the official notice for what to do.
Units affected
16,223
Official notice
2003-03-11
The hazard
The hazard
The manufacturing method for the active pharmaceutical ingredient (Scopolia extract powder) manufactured by アルプス薬品工業株式会社 and used in this product differed from the approved method. (A different extraction solvent was used.) [Specific potential health harm] We have confirmed that this product meets all approved specifications. No adverse health effects associated with this product have been reported to date.
How to check if you're affected
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.
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Turn on recall alertsAffected products
Affected products
Product 1
Units affected
Hazard
Where it was sold
Where it was sold
Retailer information is not currently available in RecallScope. Check the official notice for distribution details.
Location 1
Affected area 1
Company & contacts
Company & contacts
Brand
Manufacturer
Phone
Brand: 日本製薬工業. Contact: 連絡先 : 日本製薬工業株式会社. Phone 0568-77-4156.
Source & status
Source & status
Recall details
Recall details
Event id
Units affected
Source tier
Documents, notices & source
See the official notice and source documents for full details.
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