Public recall detail

YF-Vax powder for solution; Cracked vials

2025-08-07

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Recall Safety notice
Quick summary

Quick summary: YF-Vax powder for solution; Cracked vials. Date: 2025-08-07.

Recommended action

Recommended action: compare your product with the official notice and follow the instructions published by the official source.

Recall details

Quick summary: YF-Vax powder for solution; Cracked vials. Date: 2025-08-07.

Official details

Affected product details

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

BrandSanofi Pasteur Ltd.
ProductYF-Vax powder for solution
IssueHealth products - Packaging
Recall classType II
IdentificationRA-77821

Affected products

BrandSanofi Pasteur Ltd.
ProductYF-Vax powder for solution
DIN / NPN / authorizationDIN 00428833
Dosage formPowder For Solution
StrengthYellow fever vaccine 109648 PFU / 0.5 mL
LotUK207AA

Issue

Vials may be craked in 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 - Biologic or vaccine
CompaniesSanofi Pasteur Limited 1755 Steeles Avenue West Toronto ONTARIO M2R 3T4 CANADA
Published byHealth Canada
Recall classType II
Alert / recall typeHealth product recall
Identification numberRA-77821
Background{}
CompaniesSanofi Pasteur Limited 1755 Steeles Avenue West Toronto ONTARIO M2R 3T4 CANADA
AudiencesGeneral public Healthcare Industry
Source updated2025-08-07

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

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