Public recall detail

Atlantiscan: Broken Vials

2025-10-10

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Recall Safety notice
Quick summary

Quick summary: Atlantiscan: Broken Vials. Date: 2025-10-10.

Recommended action

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

Recall details

Quick summary: Atlantiscan: Broken Vials. Date: 2025-10-10.

Official details

Affected product details

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

BrandAtlantiscan
ProductAtlantiscan
IssueHealth products - Packaging
Recall classType I
IdentificationRA-78268

Affected products

BrandAtlantiscan
ProductAtlantiscan
DIN / NPN / authorizationDIN 02438380
Dosage formSolution
StrengthFludeoxyglucose 18F 200MCI/ML
LotF071025

Issue

The vial is broken 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 - Drugs - Radiopharmaceuticals
CompaniesNova Scotia Health Authority 1276 South Park Street Halifax, Nova Scotia B3H 2Y9
Recall date2025-10-10
Published byHealth Canada
Recall classType I
Alert / recall typeHealth product recall
Identification numberRA-78268
Background{}
CompaniesNova Scotia Health Authority 1276 South Park Street Halifax, Nova Scotia B3H 2Y9
AudiencesGeneral public Healthcare Industry
Source updated2025-10-10

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

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