Public recall detail

Jamp K8 Tablet; Out of Specification (Dissolution)

2025-03-06

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Recall Safety notice
Quick summary

Quick summary: Jamp K8 Tablet; Out of Specification (Dissolution). Date: 2025-03-06.

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 K8 Tablet; Out of Specification (Dissolution). Date: 2025-03-06.

Official details

Affected product details

Structured information extracted from the official recall notice. Confirm the identifiers and instructions in the original notice.

BrandJAMP, Jamp Pharma
ProductJamp K8 Tablet
IssueHealth products - Product quality
Recall classType II
IdentificationRA-77073

Affected products

BrandJamp Pharma
ProductJamp K8 Tablet
DIN / NPN / authorizationNPN 80013005
Dosage formTablet, Extended Release
StrengthPotassium Chloride 8.0 mEq (600 mg)
Lot800226

Issue

The dissolution is out of specification in the affected lot.

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 - Natural health products
CompaniesJAMP Pharma Corporation 1310 Nobel, Boucherville, Quebec, J4B 5H3
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-77073
Background{}
CompaniesJAMP Pharma Corporation 1310 Nobel, Boucherville, Quebec, J4B 5H3
AudiencesGeneral public Healthcare Industry
Source updated2025-03-06

Contains information licensed under the Open Government Licence – Canada. SafetyPulse is independent of the Government of Canada.

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