Home/Recalls/CANADA-82295
Health CanadaType I

Two lots of Omnitrope injectable human growth hormone recalled due to cracked cartridges

Published: July 8, 2026Recall ID: 82295Category: generalCountry: Canada
Canada
Safety AlertHealth CanadaCanadaCanada

Two lots of Omnitrope injectable human growth hormone recalled due to cracked cartridges

Recalling Firm: Communications and Public Affairs Branch

Reason for Recall / Hazard

Product quality

Product Description & Identification

If you have a recalled product, do not use it. Contact your pharmacy immediately for a replacement. Return the recalled product to your pharmacy for proper disposal.If you or your child have used this product and experience any unusual symptoms (e.g. persistent redness, swelling and/or pain at the injection site, fever) or have any other health concerns, consult a healthcare professional.Contact Sandoz Canada Inc. by calling toll-free at 1-800-343-8839 if you have questions about this recall.Report any health product-related side effects or complaints to Health Canada.

Affected Products

Omnitrope (5 mg/1.5 mL somatropin)

Additional Source Details

FieldValue
N I D82295
U R Lhttps://recalls-rappels.canada.ca/en/alert-recall/two-lots-omnitrope-injectable-human-growth-hormone-recalled-due-cracked-cartridges
IssueProduct quality
TitleTwo lots of Omnitrope injectable human growth hormone recalled due to cracked cartridges
ProductOmnitrope (5 mg/1.5 mL somatropin)
Archived0
CategoryBiologic or vaccine
Last updated2026-07-08
OrganizationCommunications and Public Affairs Branch
Recall classType I
What you should doIf you have a recalled product, do not use it. Contact your pharmacy immediately for a replacement. Return the recalled product to your pharmacy for proper disposal.If you or your child have used this product and experience any unusual symptoms (e.g. persistent redness, swelling and/or pain at the injection site, fever) or have any other health concerns, consult a healthcare professional.Contact Sandoz Canada Inc. by calling toll-free at 1-800-343-8839 if you have questions about this recall.Report any health product-related side effects or complaints to Health Canada.

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Overview

  • Recalling FirmCommunications and Public Affairs Branch
  • Risk LevelType I
Recall Hazard Severity
Caution (Class III)
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