Has Laborie Medical Technologies Corp had other FDA enforcement actions?

This is the only FDA action Argus HQ has on file for Laborie Medical Technologies Corp as of 2026-07-14. Argus ingests new FDA enforcement records daily.

What kind of FDA record is this?

This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-07-08; Argus observed and indexed it on 2026-07-14.

Where can I verify this record directly with FDA?

The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

.hq

fda_recall · device_recall · high

Laborie Medical Technologies Corp — Class II recall: Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI…

Name: FDA Recall Record — Laborie Medical Technologies Corp
Creator: Argus HQ
Published: 2026-07-08
License: https://argushq.ai/methodology

Event date: 2026-07-08 00:00:00Z
Observed: 2026-07-14 04:20:25Z
Source ID: Z-2669-2026
Payload hash: 6e26cf419347a2da858b5953…

Summary

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 perfo… Status: Ongoing.

Entities

Laborie Medical Technologies Corp

View source record ↗

Frequently asked questions

Has Laborie Medical Technologies Corp had other FDA enforcement actions?: This is the only FDA action Argus HQ has on file for Laborie Medical Technologies Corp as of 2026-07-14. Argus ingests new FDA enforcement records daily.
What kind of FDA record is this?: This is an Argus HQ record of a FDA Recall, tagged high severity by Argus HQ. FDA published the underlying record on 2026-07-08; Argus observed and indexed it on 2026-07-14.
Where can I verify this record directly with FDA?: The verbatim FDA source record is the source of truth — Argus HQ links directly to it below. Always confirm against fda.gov before acting.

Compiled by Argus HQ Research from FDA primary sources · Reviewed by Andy Gaber, Founder

Cite this record

Reusing this data in reporting or research? Here’s a ready-made citation.

APA

Argus HQ Research (2026). Laborie Medical Technologies Corp — Class II recall: Solar GI System (Water Perfusion);   Product Name (Catalog Number): Solar GI LGI…. Digital Empire LLC. Retrieved from https://argushq.ai/events/fda-recall-laborie-medical-technologies-corp-z-2669-2026

MLA

"Laborie Medical Technologies Corp — Class II recall: Solar GI System (Water Perfusion);   Product Name (Catalog Number): Solar GI LGI…." Argus HQ Research, Digital Empire LLC, 2026, argushq.ai/events/fda-recall-laborie-medical-technologies-corp-z-2669-2026.

Chicago

Argus HQ Research. "Laborie Medical Technologies Corp — Class II recall: Solar GI System (Water Perfusion);   Product Name (Catalog Number): Solar GI LGI…." Digital Empire LLC. Accessed July 14, 2026. https://argushq.ai/events/fda-recall-laborie-medical-technologies-corp-z-2669-2026.

BibTeX

@misc{argushq_argushq_ai_events_fda_recall_laborie_medical_technologies_corp_z_2669_2026_2026,
  title = {Laborie Medical Technologies Corp — Class II recall: Solar GI System (Water Perfusion);   Product Name (Catalog Number): Solar GI LGI…},
  author = {{Argus HQ Research}},
  year = {2026},
  publisher = {Digital Empire LLC},
  url = {https://argushq.ai/events/fda-recall-laborie-medical-technologies-corp-z-2669-2026},
  note = {Accessed: July 14, 2026}
}

Informational only. Not legal, financial, or medical advice.