Laborie Medical recalls Solar GI H2O systems (G3-6 to G3-14) due to moisture accumulation in pneumatic circuits that may affect airflow or pressure measurements.
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 and waterproof pressure sensors. Accumulated moisture may affect airflow or pressure measurement performance if not properly removed.
Laborie Medical is recalling Solar GI H2O water perfusion systems (G3-6 to G3-14) because moisture can build up in the internal tubing or sensors during long-term use, potentially causing inaccurate airflow or pressure readings.
Moisture can accumulate in the pneumatic circuit's internal tubing or hydrophobic filters during long-term use. This may lead to inaccurate airflow or pressure measurements if not properly managed, though it does not cause immediate harm.
Healthcare facilities using Solar GI H2O systems for medical water perfusion are affected. Patients and staff using these systems during extended procedures may be at slightly higher risk due to potential measurement errors.
Check for the catalog numbers G3-6 through G3-14 on the Solar GI H2O system. All serial numbers are affected across these models.
Identify the catalog number on your Solar GI H2O system to confirm if it is in the affected range (G3-6 to G3-14).
No immediate danger is expected. The recall addresses potential measurement inaccuracies during long-term use, not immediate injury risks.
Check the catalog number on your system; affected models are G3-6 through G3-14. All serial numbers are included in this recall.
No. The recall does not require stopping use; it addresses potential measurement issues that can be managed with proper maintenance.
We’ve drafted a message you can send Laborie Medical to request your refund or repair — edit it as you like.
Subject: Recall Z-2669-2026 — Laborie Medical Laborie Medical Hello, I own a Laborie Medical that is covered by recall Z-2669-2026 from Laborie Medical. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
