Public recall detail

JAMP Pantoprazole Sodium: oversized tablets

2024-07-25

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Recall Safety notice
Quick summary

Quick summary: JAMP Pantoprazole Sodium: oversized tablets. Date: 2024-07-25.

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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