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Official recall record

Sight OLO Test Kit

Health Canada — Medical Devices · 2024-06-05 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2024-06-05
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

One test kit lot (TK1-10114) shows a positive bias in the platelet count due to bacterial contamination which can result in elevated counts with a bias of 7.5 k/uL. This results in the test kit lot performing outside of the device specification. Recall Start Date: May 15, 2024

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.