Cook Incorporated
750 DANIELS WAY, Bloomington, IN, US
Registered product codes
202 product codes
Recent MDR events
1,316 on file
- OlsenJul 30, 2026Malfunction50082356
- InstinctJul 28, 2026Malfunction50053114
- BEACON TIP TORCON NBJul 14, 2026Malfunction25811926
- COOKJul 14, 2026Malfunction25812152
- COOKJul 9, 2026Malfunction25762767
- INSTINCTJul 8, 2026Malfunction25746752
- INSTINCTJul 8, 2026Malfunction25746848
- FLEXORJun 30, 2026Malfunction25665195
- WAYNE PNEUMOTHORAX TRAYJun 22, 2026Malfunction25576224
- COOK MEDICAL MICROPUNCTURE INTRODUCER SETJun 17, 2026InjuryMW5189588
Recalls
85 on file
- Open, ClassifiedMay 1, 2026
Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.
View FDA record ↗ - Open, ClassifiedMay 1, 2026
Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.
View FDA record ↗ - Open, ClassifiedMay 1, 2026
Marker bands may be at an increased risk of cracking/breakage. Potential adverse events that may result include increased procedural time, harms associated with device fragmentation/separation, and vessel injury. In a worst-case scenario, device fragmentation and separation may cause life-threatening harm or death.
View FDA record ↗ - Open, ClassifiedApr 6, 2026
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
View FDA record ↗ - Open, ClassifiedApr 6, 2026
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
View FDA record ↗ - Open, ClassifiedApr 6, 2026
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
View FDA record ↗ - Open, ClassifiedApr 6, 2026
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
View FDA record ↗ - Open, ClassifiedApr 6, 2026
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
View FDA record ↗ - Open, ClassifiedApr 6, 2026
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
View FDA record ↗ - Open, ClassifiedApr 6, 2026
Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.
View FDA record ↗
Compliance history
Matched by FEI 1820334.
FDA inspections
3 on file
- Voluntary Action Indicated (VAI)Jun 4, 2025
Compliance: Devices · Citations posted
- Voluntary Action Indicated (VAI)Jun 4, 2025
Postmarket Assurance: Devices · Citations posted
- Voluntary Action Indicated (VAI)May 8, 2024
Compliance: Devices · Citations posted
Inspection citations
7 on file
Top cited requirements
Compare to industry ↗21 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
221 CFR 820.100(a)Lack of or inadequate procedures
221 CFR 820.70(c)Environmental control Lack of or inadequate procedures
121 CFR 820.70(g)Equipment Installation, Placement, Specified Requirements
121 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
1
- 21 CFR 820.70(a)Jun 4, 2025
Process control procedures, Lack of or inadequate procedures
- 21 CFR 820.70(a)Jun 4, 2025
Production processes
- 21 CFR 820.70(c)Jun 4, 2025
Environmental control Lack of or inadequate procedures
- 21 CFR 820.70(g)Jun 4, 2025
Equipment Installation, Placement, Specified Requirements
- 21 CFR 820.75(b)Jun 4, 2025
Lack/Inad procedure-Monitoring/Control of Validated Proces
- 21 CFR 820.100(a)Jun 4, 2025
Lack of or inadequate procedures
- 21 CFR 820.100(a)May 8, 2024
Lack of or inadequate procedures
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.