ProductGuru Recalls

Official recall record

Aesculap unlicenced medical devices

Health Canada — Medical Devices · 2026-01-15 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2026-01-15
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Internal review found 82 medical devices imported to Canada without an appropriate license by Health Canada. All are safe, effective, and meet manufacturer standards. No risk to patients, users, or third parties is present. No immediate actions by the end users required.

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.

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