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Solar™ gi
Official notice
16 Jul 2026
Last checked
16 Jul 2026
An official Health Canada notice concerns Solar™ gi. Under extended clinical use conditions (e.g., long-duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the hydrophobic filter (part of MPP T/PC tubing set) and pressure sensors. Accumulated moisture may affect airflow or pressure measurement performance if not properly removed. Water ingress in the air compressor can cause inaccurate pressure readings, resulting in excess fluid being administered to the patient than what is indicated by the system, which can lead to patient water intoxication. The issue is only related to Solar GI systems that have water perfusion capabilities. Published 2026-07-16.
What to do now
Contact the manufacturer if you require additional information.
Recall number
82331
Official notice
2026-07-16
The hazard
The hazard
Under extended clinical use conditions (e.g., long-duration studies), moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the hydrophobic filter (part of MPP T/PC tubing set) and pressure sensors. Accumulated moisture may affect airflow or pressure measurement performance if not properly removed. Water ingress in the air compressor can cause inaccurate pressure readings, resulting in excess fluid being administered to the patient than what is indicated by the system, which can lead to patient water intoxication. The issue is only related to Solar GI systems that have water perfusion capabilities.
How to check if you're affected
How to check if you're affected
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Brand: Laborie Medical.
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See the official notice and source documents for full details.
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