Quick summary: JAMP Pantoprazole Sodium: oversized tablets. Date: 2024-07-25.
Public recall detail
JAMP Pantoprazole Sodium: oversized tablets
2024-07-25
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 Pantoprazole Sodium: oversized tablets. Date: 2024-07-25.
Official details
Affected product details
Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.
BrandJAMP
ProductJAMP Pantoprazole Sodium
IssueHealth products - Product safety
Recall classType II
IdentificationRA-75869
Affected products
BrandJAMP
ProductJAMP Pantoprazole Sodium
DIN / NPN / authorizationDIN 02392623
Dosage formTablet (Delayed-Release)
StrengthPANTOPRAZOLE (PANTOPRAZOLE SODIUM SESQUIHYDRATE) 40mg
LotEG24PAM001
Issue
The affected lot may contain oversized tablets.
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 Nobel, Boucherville, Quebec, J4B 5H3
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-75869
Background{}
CompaniesJAMP Pharma Corporation 1310 Nobel, Boucherville, Quebec, J4B 5H3
AudiencesGeneral public Healthcare Industry
Source updated2024-07-25
Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.
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