How many FDA warning letters has Katalyst Surgical, LLC received?

Argus HQ has not recorded an FDA warning letter for Katalyst Surgical, LLC in our current dataset.

What FDA recalls has Katalyst Surgical, LLC issued?

Argus HQ has recorded 12 FDA recalls tied to Katalyst Surgical, LLC.

Is Katalyst Surgical, LLC FDA compliant?

Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 12 recalls, and 0 approval records for Katalyst Surgical, LLC. Review the linked FDA source records directly before drawing a compliance conclusion.

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company

Katalyst Surgical, LLC

Name: FDA Enforcement Actions Against Katalyst Surgical, LLC
Creator: Argus HQ
License: https://argushq.ai/methodology

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_recall2026-05-13
Katalyst Surgical, LLC — Class II recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Asymmetrical Tano Forceps, Model/C…
fda_recall · device_recall2026-05-13
Katalyst Surgical, LLC — Class II recall: DEX Ophthalmic Tissue Forceps, 23ga DEX Maculorhexis Forceps, Model/Catalog Numb…
fda_recall · device_recall2026-05-13
Katalyst Surgical, LLC — Class II recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff End Grasping Forceps, Model/Catalo…
fda_recall · device_recall2026-05-13
Katalyst Surgical, LLC — Class II recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Super Grip Forceps, Model/Catalog Number…
fda_recall · device_recall2026-05-13
Katalyst Surgical, LLC — Class II recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Maculorhexis Forceps, Model/Catalog Numb…
fda_recall · device_recall2026-05-13
Katalyst Surgical, LLC — Class II recall: DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Super Grip Forceps, Model/Catalog…
fda_recall · device_recall2026-05-13
Katalyst Surgical, LLC — Class II recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Nano Tapered AWH Forceps, Model/Catalog…
fda_recall · device_recall2026-05-13
Katalyst Surgical, LLC — Class II recall: DEX Ophthalmic Tissue Forceps, 23ga DEX NanoTapered AWH Forceps, Model/Catalog N…
fda_recall · device_recall2026-05-13
Katalyst Surgical, LLC — Class II recall: DEX Ophthalmic Tissue Forceps, 27ga DEX Stiff Maculorhexis Forceps, Model/Catalo…
fda_recall · device_recall2026-05-13
Katalyst Surgical, LLC — Class II recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Super Grip Forceps, Model/Catalog…
fda_recall · device_recall2026-05-13
Katalyst Surgical, LLC — Class II recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Maculorhexis Forceps, Model/Catalo…
fda_recall · device_recall2026-05-13
Katalyst Surgical, LLC — Class II recall: DEX Ophthalmic Tissue Forceps, 25ga DEX Stiff Serrated Forceps, Model/Catalog Nu…

Frequently asked questions

How many FDA warning letters has Katalyst Surgical, LLC received?: Argus HQ has not recorded an FDA warning letter for Katalyst Surgical, LLC in our current dataset.
What FDA recalls has Katalyst Surgical, LLC issued?: Argus HQ has recorded 12 FDA recalls tied to Katalyst Surgical, LLC.
Is Katalyst Surgical, LLC FDA compliant?: Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 12 recalls, and 0 approval records for Katalyst Surgical, LLC. 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.