company
Cook Incorporated
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_recall2026-05-13Cook Incorporated — Class I recall: Aurous Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20-01 GPN G473…
- fda_recall · device_recall2026-05-13Cook Incorporated — Class I recall: Centimeter Sizing Catheter RPN N5.0-35-100-P-10S-PIG-CSC-20 GPN G11916 Cath…
- fda_recall · device_recall2026-05-13Cook Incorporated — Class I recall: Beacon Tip Centimeter Sizing Catheter RPN/GPN NR5.0-35-70-P-10S-0-CSC-20 G312…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Approach CTO-18 Micro Wire Guide, Reference Part Number CMW-14-190-…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL NCompass¿ Nitinol Stone Extractor: Reference Part Number C-NTSE-2.…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Ciaglia Blue Rhino Percutaneous Tracheostomy Introducer Set: Refer…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Spectrum¿ Central Venous Catheter Set: Reference Part Number C-UDL…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: Melker Universal Cuffed Emergency Cricothyrotomy Catheter Set: Reference Part N…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Wayne Pneumothorax Set: Reference Part Number C-UTPT-1020-WAYNE-IM…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Cook Staged Extubation Set: Reference Part Number C-CAE-14.0-83-EX…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Cook¿ Strange Bile Duct Stone Exploration Set: Reference Part Numb…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Approach CTO-6 Micro Wire Guide, Reference Part Number CMW-14-190-6…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Cook¿ Spectrum¿ Central Venous Catheter Tray: Reference Part Numbe…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Wayne Pneumothorax Tray: Reference Part Number C-UTPTY-1400-WAYNE-…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Arterial Pressure Monitoring Tray, Reference Part Number APMY-2.5-1…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Spectrum¿ Central Venous Tray: Reference Part Number C-UQLMYJ-1001…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Multipurpose Drainage Catheter: Reference Part Number ULT8.5-38-25…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Approach CTO-12 Micro Wire Guide: Reference Part Number CMW-14-19…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Blue Rhino¿ G2-Multi Percutaneous Tracheostomy Introducer Tray: Re…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Blue Rhino G2-Multi Percutaneous Tracheostomy Introducer Set: Refe…
- fda_recall · device_recall2026-04-15Cook Incorporated — Class II recall: COOK MEDICAL Thal-Quick Chest Tube Tray: Reference Part Number C-TQTSY-3200, Or…
Frequently asked questions
- How many FDA warning letters has Cook Incorporated received?
- Argus HQ has not recorded an FDA warning letter for Cook Incorporated in our current dataset.
- What FDA recalls has Cook Incorporated issued?
- Argus HQ has recorded 21 FDA recalls tied to Cook Incorporated.
- Is Cook Incorporated FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 21 recalls, and 0 approval records for Cook Incorporated. 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.