ProductGuru Recalls

Official recall record

Osstell® Smartpeg Type 101-104

Health Canada — Medical Devices · 2025-07-17 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-07-17
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

If not correctly used with a reference measurement on implant level. The measurement on abutment can indicate a false high ISQ value. This can influence the clinician to take the wrong decision and load the implant too early, in the extension potentially resulting in implant failure for the patient. Recall start date: May 23, 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.

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ProductGuru Recalls republishes official safety information with attribution. We are not the issuing authority and this page is not advice. If this product is a medical device or medication, speak to a doctor or pharmacist. Found an error? Report it — corrections are published.