Home/Recalls/CANADA-75398
Health CanadaType I

PMS-Duloxetine 60 mg: Exceeds acceptable interim intake limit for N-nitroso-dulo...

Published: April 17, 2024Recall ID: 75398Category: generalCountry: Canada

Reason for Recall / Hazard

Product quality

Product Description & Identification

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.

Affected Products

PMS-Duloxetine 60 mg

Additional Source Details

FieldValue
N I D75398
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/pms-duloxetine-60-mg-exceeds-acceptable-interim-intake-limit-n-nitroso-duloxetine-ndlx
IssueProduct quality
TitlePMS-Duloxetine 60 mg: Exceeds acceptable interim intake limit for N-nitroso-duloxetine (NDLX)
ProductPMS-Duloxetine 60 mg
Archived0
CategoryDrugs
Last updated2024-04-17
OrganizationDrugs and health products
Recall classType I
What you should doVerify 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.

Overview

  • Recalling FirmDrugs and health products
  • Risk LevelType I
Official Agency Alert