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Atlantiscan: Broken Vials
Last updated
Summary
Product
Atlantiscan
Issue
Health products - Packaging
What to do
Consult your health care professional if you have any health concerns.
Affected products
Brand |
Product Name |
Market Authorization |
Dosage Form |
Strength |
Lot |
|---|---|---|---|---|---|
Atlantiscan |
Atlantiscan |
DIN 02438380 |
Solution |
Fludeoxyglucose 18F 200MCI/ML |
F071025 |
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 information
Background
Depth of Recall: End users
Details
Original published date:
Alert / recall type
Health product recall
Category
Health products - Drugs - Radiopharmaceuticals
Companies
Nova Scotia Health Authority
1276 South Park Street
Halifax, Nova Scotia
B3H 2Y9
Published by
Health Canada
Audience
General public
Healthcare
Industry
Recall class
Type I
Recall date
Identification number
RA-78268
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