Quick summary: JAMP-Risperidone 0.25mg: Out of specification (Stability). Date: 2025-11-19.
Public recall detail
JAMP-Risperidone 0.25mg: Out of specification (Stability)
2025-11-19
Recall
Safety notice
Quick summary
Recommended action
Recommended action: compare your product with the official notice and follow the instructions published by the official source.
Recall details
Quick summary: JAMP-Risperidone 0.25mg: Out of specification (Stability). Date: 2025-11-19.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandJAMP
ProductJAMP-Risperidone 0.25mg
IssueHealth products - Product quality
Recall classType III
IdentificationRA-81247
Affected products
BrandJAMP
ProductJAMP-RISPERIDONE
DIN / NPN / authorizationDIN 02359529
Dosage formTablet
StrengthRisperidone 0.25mg
LotENN063001, ENN062001
Issue
The impurities are out of specification during stability in the affected lots.
What you should do
- Verify if your product is affected.
- Consult your healthcare provider prior to discontinuing use of the affected product(s), or for any health concerns.
- Contact the recalling firm if you have any questions about the recall.
- Report any health product related side effects to Health Canada.
- Report any other health product safety complaints to Health Canada.
Additional official information
AudienceGeneral public Healthcare Industry
CategoryHealth products - Drugs
CompaniesJAMP Pharma Corporation 1310 Rue Nobel Boucherville, Quebec Canada J4B 5H3
Recall date2025-11-19
Published byHealth Canada
Recall classType III
Alert / recall typeHealth product recall
Identification numberRA-81247
Background{}
CompaniesJAMP Pharma Corporation 1310 Rue Nobel Boucherville, Quebec Canada J4B 5H3
AudiencesGeneral public Healthcare Industry
Source updated2025-11-19
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
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