Public recall detail

JAMP-Cetirizine: Impurity

2021-11-09

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Recall Safety notice
Quick summary

Quick summary: JAMP-Cetirizine: Impurity. Date: 2021-11-09.

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-Cetirizine: Impurity. Date: 2021-11-09.

Official details

Affected product details

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

BrandJAMP-Cetirizine
ProductJAMP-Cetirizine
IssueHealth products - Product quality
Recall classType II
IdentificationRA-63567

Affected products

BrandJAMP-Cetirizine
ProductJAMP-Cetirizine 10 mg
DIN / NPN / authorizationDIN 02451778
Dosage formTablet
StrengthCetirizine Hydrochloride 10 mg
LotMC19004C
BrandJAMP-Cetirizine
ProductJAMP-Cetirizine 20 mg
DIN / NPN / authorizationDIN 02466171
Dosage formTablet
StrengthCetirizine Hydrochloride 20 mg
LotMC20005B, MC20006

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 Health professionals Hospitals
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-63567
Background{}
CompaniesJamp Pharma Corporation. 1310 Nobel, Boucherville, Quebec, J4B 5H3
AudiencesGeneral public Health professionals Hospitals
Source updated2021-11-09

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

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