Official recall record
Karl Storz Sets
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2025-08-28
- Last updated (per notice)
- 2025-08-27
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Upon internal review, it was identified that some products, including sets containing unlicensed components, were sold over a period of time without the appropriate licensing in place. This recall is not related to any safety or performance concerns. There is no risk to patients or users. Customers may continue to use the product as usual. Recall start date: August 13, 2025
What to do
Follow the instructions in the official notice — recall remedies (refund, repair, replacement, or disposal) are defined by the issuing authority and the responsible business, and they differ per recall. Do not rely on summaries, including this one.
Verify at the source:
Health Canada — Medical Devices — official record →
Record last checked against the registry on 2026-05-31.
Record last checked against the registry on 2026-05-31.
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