company
Avanos Medical, Inc.
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_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6316
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Brand Name: CORFLO Product Name: CORFLO Safety PEG Kit Model/Catalog Number: 3…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUS…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUL…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUS…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Brand Name: CORFLO Product Name: CORFLO* Safety PEG Kit Model/Catalog Number:…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 20 Fr PUL…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUS…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: CORFLO* Safety PEG Kit with ENFit¿ Connector Model/Catalog Number…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 14 Fr PUL…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: CORFLO Safety PEG Kit with ENFit Connector Model/Catalog Number:…
- fda_recall · device_recall2026-06-17Avanos Medical, Inc. — Class II recall: Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit with ENFit…
Frequently asked questions
- How many FDA warning letters has Avanos Medical, Inc. received?
- Argus HQ has not recorded an FDA warning letter for Avanos Medical, Inc. in our current dataset.
- What FDA recalls has Avanos Medical, Inc. issued?
- Argus HQ has recorded 20 FDA recalls tied to Avanos Medical, Inc..
- Is Avanos Medical, Inc. FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 20 recalls, and 0 approval records for Avanos Medical, Inc.. 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.