How many FDA warning letters has Laborie Medical Technologies Corp received?

Argus HQ has not recorded an FDA warning letter for Laborie Medical Technologies Corp in our current dataset.

What FDA recalls has Laborie Medical Technologies Corp issued?

Argus HQ has recorded 1 FDA recall tied to Laborie Medical Technologies Corp.

Is Laborie Medical Technologies Corp FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for Laborie Medical Technologies Corp. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Laborie Medical Technologies Corp

Name: FDA Enforcement Actions Against Laborie Medical Technologies Corp
Creator: Argus HQ
License: https://argushq.ai/methodology

Industry: Medical Devices

Jurisdiction: US

FDA Warning Letter timeline

V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.

fda_recall · device_recall2026-07-08
Laborie Medical Technologies Corp — Class II recall: Solar GI System (Water Perfusion); Product Name (Catalog Number): Solar GI LGI…

Frequently asked questions

How many FDA warning letters has Laborie Medical Technologies Corp received?: Argus HQ has not recorded an FDA warning letter for Laborie Medical Technologies Corp in our current dataset.
What FDA recalls has Laborie Medical Technologies Corp issued?: Argus HQ has recorded 1 FDA recall tied to Laborie Medical Technologies Corp.
Is Laborie Medical Technologies Corp FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 1 recall, and 0 approval records for Laborie Medical Technologies Corp. Review the linked FDA source records directly before drawing a compliance conclusion.

Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.