Lower risk Medical device recall · FDA · Published May 21, 2026

Laborie Solar GI System Recall: Moisture Risk in Pneumatic Circuits

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.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-2669-2026Medical device Laborie Medical ›

Lower-risk recall

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.

Take action

Contact the company

Recalling firmLaborie Medical Technologies Corp180 International Dr · Portsmouth, NH 03801-6837

✎ GovInfoNow plain-language explainer

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. Read more at govinfonow.com/recall/49123-laborie-solar-gi-system-recall-moisture-risk-in-pneumatic-circuits.

Source Summary by GovInfoNow · govinfonow.com/recall/49123-laborie-solar-gi-system-recall-moisture-risk-in-pneumatic-circuits · Updated August 10, 2026 · FDA enforcement record: FDA #Z-2669-2026

Cite this page

“Laborie Solar GI System Recall: Moisture Risk in Pneumatic Circuits.” GovInfoNow, updated August 10, 2026. https://govinfonow.com/recall/49123-laborie-solar-gi-system-recall-moisture-risk-in-pneumatic-circuits. Based on FDA recall #Z-2669-2026 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2669-2026%22&limit=1).

The FDA announced on May 21, 2026, that Laborie Medical Technologies Corp is recalling the Solar GI System (Water Perfusion) due to potential moisture accumulation affecting performance. The agency issued recall number Z-2669-2026 for the voluntary Class II recall.

How to tell if you have it

Brand: Laborie Medical
Product Name: Solar GI LGI H2O, 12p, Trolley system (G3-6), Solar GI HRM H2O, 24p, Compact Pole system (G3-7), Solar GI HRM H2O, 24p, Trolley system (G3-8), Solar GI HRM H2O, 36p, Trolley system (G3-12), Solar GI HRAM H2O, 24p, Trolley system (G3-14)
Catalog Numbers: G3-6, G3-7, G3-8, G3-12, G3-14
Primary UDI-DI: 08717775955047, 08717775955054, 08717775955061, 08717775955078, 08717775955085
Basic UDI-DI: 87177759500G3G8
Quantity: 372 units

The hazard

According to the FDA, moisture generated within the pneumatic circuit may accumulate inside the system's internal tubing or at the hydrophobic filter and waterproof pressure sensors during extended clinical use. This accumulation may affect airflow or pressure measurement performance if not properly removed.

Context

GovInfoNow's records show Laborie Medical Technologies Corp has one other recall on record since July 17, 2019: the Solar Blue Laptop Power Supply Recall for fire hazard risk. Other recent recalls of similar products include Olympus UHI-3 Insufflation Unit Recall (Jan. 16, 2026), Medline medical procedure kits with Strykeflow 2 irrigation leak risk (Dec. 16, 2025), and Olympus UHI-2 Insufflation Unit Recall (Jan. 16, 2026).

How to tell if you have this one

Check for the catalog numbers G3-6 through G3-14 on the Solar GI H2O system. All serial numbers are affected across these models.

Brand
Laborie Medical
Category
Medical device

Based on the official FDA remedy

What to do — step by step

Check System Model
Identify the catalog number on your Solar GI H2O system to confirm if it is in the affected range (G3-6 to G3-14).

Where it went and when

Where it was distributed

Distributed nationwide, and outside the U.S.

FDA distribution: “Worldwide distribution - US Nationwide and the countries of Argentina, Australia, Austria, Bangladesh, Belgium, Canada, China, Costa Rica, Croatia, Cyprus, Czech Republic. Denmark, Egypt, France, Germany, Hong Kong, Hungary, India,…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Distributed nationwide, and outside the U.S.

Recall timeline

FDA published this recall 48 days after the firm started it.

May 21, 2026Firm started the recall
Jul 2, 2026FDA classified it Class II
Jul 8, 2026Published in FDA’s Enforcement Report

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

Is this recall dangerous?

No immediate danger is expected. The recall addresses potential measurement inaccuracies during long-term use, not immediate injury risks.

Do I need to stop using the system?

No. The recall does not require stopping use; it addresses potential measurement issues that can be managed with proper maintenance.

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Link to this recall

<a href="https://govinfonow.com/recall/49123-laborie-solar-gi-system-recall-moisture-risk-in-pneumatic-circuits">Laborie Solar GI System Recall: Moisture Risk in Pneumatic Circuits (GovInfoNow)</a>

Where this comes from

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.

Official source: FDA Recall #Z-2669-2026 (May 21, 2026) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-2669-2026 to see it in context.
Plain-language summary written by qwen3:4b on August 10, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.