Health CanadaType I

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

Veröffentlicht: 8. Juli 2026Rückruf-ID: 82295Kategorie: VerbraucherprodukteLand: Kanada
Canada
Safety AlertHealth CanadaCanadaCanada

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

Recalling Firm: Communications and Public Affairs Branch

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Grund für den Rückruf / Gefahr

Product quality

Produktbeschreibung & Identifikation

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.

Betroffene Produkte

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.

Consumer Action Protocol: What You Should Do Immediately

Safety Steps
1Verify Product Identifiers

Check the model number, serial number, and date stamp on the rating label on the back or underside of the product.

2Isolate & Discontinue Use

Immediately discontinue using the product. Unplug electrical items and keep juvenile items out of reach of children.

3Claim Free Statutory Remedy

Under statutory consumer protection rules, consumers are entitled to a full refund, certified replacement, or free repair kit without needing the original sales receipt.

4Report Adverse Incidents

If you suffered an injury, illness, or property damage from this product, file an official incident report with regulatory authorities (Health Canada).

Your Legal Rights as a Consumer

Recalls are legally binding corrective safety actions overseen by statutory government bodies. Recalling entities are legally prohibited from charging consumers for official safety remedies. If a retailer or dealership refuses your recall remedy, notify the issuing regulatory agency immediately.

Frequently Asked Questions About This Recall

FAQ Guide

Q1:What should I do immediately if I own or bought Two lots of Omnitrope injectable human growth hormone recalled due to cracked cartridges?

Immediately stop using the product and keep it out of reach of children. Disconnect power if electrical, and do not attempt makeshift home repairs.

Q2:Can I get a full refund or free repair for this recall?

Yes. Recalling manufacturers and retail merchants are required under consumer protection regulations to offer a statutory remedy—typically a full refund, certified repair kit, or replacement unit.

Q3:Do I need my original sales receipt to claim a remedy or refund?

In most recall cases, no receipt is required. Because safety recalls are matters of public health and statutory compliance, retailers and manufacturers routinely issue refunds, store credit, or replacement kits upon presentation of the affected product or lot code.

Q4:Where can I verify official information for this safety alert?

This safety alert is aggregated directly from official regulatory agency records (Health Canada). You can click the 'Official Agency Alert' link on this page to view the primary government notice and contact the manufacturer directly.

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Übersicht

  • Rückrufendes UnternehmenCommunications and Public Affairs Branch
  • RisikostufeType I
Recall Hazard Severity
Caution (Class III)
Offizielle Behördenwarnung

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