Public recall detail

Limited number of Sarclisa single use vials may have been frozen during shipment

2026-09-25

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Health products Health product recall
Quick summary

Quick summary: Limited number of Sarclisa single use vials may have been frozen during shipment. Reason: Health product recall. Category: Health products. Date: 2026-09-25.

Recommended action

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

Recall details

Quick summary: Limited number of Sarclisa single use vials may have been frozen during shipment. Reason: Health product recall. Category: Health products. Date: 2026-09-25.

Official details

Affected product details

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

BrandSanofi-Aventis Canada Inc., Sarclisa
ProductSARCLISA
IssueHealth products - Product quality
Recall classType I
IdentificationRA-82683

Affected products

BrandSarclisa
ProductSarclisa
DIN / NPN / authorizationDIN 02498243
Dosage formSingle-use vial
Strength500 mg/25 mL
Lot5F028A

Issue

Units of the affected lot may have been frozen during shipping. Only nine (9) units from the lot are being recalled from three (3) locations in Nova Scotia.

What you should do

  • Only a limited number of units within the lot are affected by this recall. Do not assume your product is affected solely because the lot number appears in the table.
  • Consult your healthcare provider 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-aventis Canada Inc. 1755 Steeles Ave. West Toronto, ON M2R 3T4
Recall date2026-09-23
DistributionNova Scotia
Published byHealth Canada
Recall classType I
Alert / recall typeHealth product recall
Identification numberRA-82683
Background{}
CompaniesSanofi-aventis Canada Inc. 1755 Steeles Ave. West Toronto, ON M2R 3T4
AudiencesGeneral public Healthcare Industry
Source updated2026-09-25

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

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