Official recall record
OsmoPRO® MAX Automated Osmometer
- Issuing authority
- Health Canada — Medical Devices
- Published
- 2024-03-25
- Last updated (per notice)
- 2024-03-22
- Country of alert
- Canada
- Alert level
- Type II
- Alert type
- recall
What the authority reported
Advanced instruments is issuing a recall for the device due to two issues: 1) system error messages that may delay the ability to test patient samples 2) the need for frequent calibration due to results outside the expected range when testing controls. Recall start date: March 11, 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.
Record last checked against the registry on 2026-05-31.
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