ProductGuru Recalls

Official recall record

Eclipse™ Pro and Eclipse™ Mini

Health Canada — Medical Devices · 2025-01-08 · CanadaType II
Issuing authority
Health Canada — Medical Devices
Published
2025-01-08
Country of alert
Canada
Alert level
Type II
Alert type
recall

What the authority reported

Eclipse™ Pro 98700 and Eclipse™ Mini 98900 devices may have mismatched serial numbers between the label and what is programmed in the devices. This is due to a process error on the manufacturing line, which has resulted in an incorrect serial number being set in a small number of the devices. We are notifying all customers using the devices and providing guidelines to ensure this mismatch does not result in any unreasonable risk. Recall start date: December 27, 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.