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COOK INCORPORATED

United States·US-MF-000003180

Last updated September 17, 2026

Information

Country
United States
Address
750 Daniels Way, Bloomington, United States
LinkedIn
—
Facebook
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Phone
+1-812-339-2235
PRRC Contact
—
EUDAMED SRN
US-MF-000003180
FDA FEI Number
1825146
DUNS Number
079720472

Catalogue (9678)

Page 9 of 194
DeviceModel / ReferenceRegistriesClassStatus
Zenith Flex G48433
FDA UDI
Class IIIActive
Cook G57624
FDA UDI
Class IIActive
Rhapsody H-30 G47625
FDA UDI
Class IIActive
Nester G47358
FDA UDI
Class IIActive
Cook G00063
FDA UDI
Class IIActive
Robinson G17025
FDA UDI
Class IIActive
Cook G14530
FDA UDI
Class IIActive
Cook G06600
FDA UDI
Class IIActive
Ring-McLean G07224
FDA UDI
Class IActive
Cope G04640
FDA UDI
Class IIActive
Universa G23400
FDA UDI
Class IIActive
Cook G58881
FDA UDI
Class IIActive
Sof-Flex G14865
FDA UDI
Class IIActive
Torcon NB G27702
FDA UDI
Class IIActive
Cook G07173
FDA UDI
Class IIActive
Turbo-Ject G34521
FDA UDI
Class IIUnknown
Torcon NB G47110
FDA UDI
Class IIActive
Passport G22615
FDA UDI
Class IIUnknown
Universa G23239
FDA UDI
Class IIActive
MReye G20388
FDA UDI
Class IIActive
Cook G00875
FDA UDI
Class IIActive
Flexor G30393
FDA UDI
Class IIActive
Cook G05089
FDA UDI
Class IIActive
Greene G16226
FDA UDI
Class IIUnknown
Advance G30876
FDA UDI
Class IIActive
Advance G30860
FDA UDI
Class IIActive
MReye G42394
FDA UDI
Class IIActive
Cook G15753
FDA UDI
Class IIActive
Nester G52750
FDA UDI
Class IIActive
Cook G46246
FDA UDI
Class IIActive
Torcon NB G27713
FDA UDI
Class IIActive
Cook G00104
FDA UDI
Class IIActive
Cook G24806
FDA UDI
Class IIActive
Cook Spectrum G47845
FDA UDI
Class IIActive
Cook G57468
FDA UDI
UActive
Cook G28956
FDA UDI
Class IIActive
Lunderquist-Ring G27887
FDA UDI
Class IIActive
Torcon NB G47182
FDA UDI
Class IIActive
Cook G46429
FDA UDI
Class IIActive
Nester G23535
FDA UDI
Class IIActive
Ascend AQ G32831
FDA UDI
Class IIActive
Cook G58879
FDA UDI
Class IIActive
Cook G58858
FDA UDI
Class IIActive
Universa G49948
FDA UDI
Class IIActive
High-Flo Silver G03072
FDA UDI
Class IIActive
Tornado G47519
FDA UDI
Class IIActive
Cook Spectrum G10042
FDA UDI
Class IIActive
Entuit G47290
FDA UDI
Class IIActive
Cook G10019
FDA UDI
Class IIActive
Cook G16156
FDA UDI
NUnknown

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Importers

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Notified Bodies

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Authorities

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FDA Recalls (85)

Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.

DateRecall No.ClassStatusReason
Apr 2, 2026Z-1936-2026—open, classified

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.

Apr 2, 2026Z-1934-2026—open, classified

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.

Apr 2, 2026Z-1935-2026—open, classified

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.

Mar 5, 2026Z-1785-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1787-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1781-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1792-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1777-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1783-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1788-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1784-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1775-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1779-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1790-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1780-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1776-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1789-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1778-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1786-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1791-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Mar 5, 2026Z-1782-2026—open, classified

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Nov 26, 2025Z-0995-2026—open, classified

Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.

Nov 26, 2025Z-0993-2026—open, classified

Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.

Nov 26, 2025Z-0994-2026—open, classified

Cook Medical identified that products supplied in the affected device lots may have been manufactured out of specification. Impacted products may have been cut to the incorrect length, not correctly trimmed, and not inspected properly.

May 15, 2025Z-1902-2025—open, classified

Cook Medical identified that catheters supplied in the affected device lots may experience tip separation.

Apr 17, 2025Z-1786-2025—open, classified

Cook Medical identified that devices from the affected device lots may contain the incorrectly sized introducer sheath.

Apr 17, 2025Z-1762-2025—open, classified

Cook Medical identified that devices from the affected device lots may contain the incorrectly sized embolization coil.

Apr 17, 2025Z-1787-2025—open, classified

Cook Medical identified that devices from the affected device lots may contain the incorrectly sized introducer sheath.

Oct 14, 2024Z-0499-2025—open, classified

Devices from the affected device lots have labels that state the incorrect expiration dates.

Oct 8, 2024Z-0347-2025—open, classified

Affected device lots have labels that state the incorrect expiration dates.

Oct 8, 2024Z-0346-2025—open, classified

Affected device lots have labels that state the incorrect expiration dates.

Sep 16, 2024Z-0045-2025—open, classified

Cook Medical is conducting removal of a lot of Check-Flo Performer Introducer Set due to complaints that the white caps that connect the shaft to the hub of these products may disconnect.

May 15, 2024Z-2222-2024—open, classified

Product labels state the incorrect expiration dates that extends beyond their true expiration date

May 15, 2024Z-2223-2024—open, classified

Product labels state the incorrect expiration dates that extends beyond their true expiration date

Mar 1, 2024Z-1532-2024—open, classified

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Mar 1, 2024Z-1528-2024—open, classified

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Mar 1, 2024Z-1525-2024—open, classified

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Mar 1, 2024Z-1531-2024—open, classified

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Mar 1, 2024Z-1530-2024—open, classified

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Mar 1, 2024Z-1529-2024—open, classified

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Mar 1, 2024Z-1526-2024—open, classified

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Mar 1, 2024Z-1527-2024—open, classified

Packaging may have low seal strength and not meet peel strength specifications, compromising device sterility

Apr 7, 2023Z-1428-2023—open, classified

There were reports from customers that the tracheostomy in the sets and trays is not making a secure connection with the 15mm cap and other 15mm circuit components and accessories. This resulted in an unsecure connection between the device connector and circuit components, cap, or accessories.

Apr 7, 2023Z-1427-2023—open, classified

There were reports from customers that the tracheostomy in the sets and trays is not making a secure connection with the 15mm cap and other 15mm circuit components and accessories. This resulted in an unsecure connection between the device connector and circuit components, cap, or accessories.

Aug 16, 2022Z-1847-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1831-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1834-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1838-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1836-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1829-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1841-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1825-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1844-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1845-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1824-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1843-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1842-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1835-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1826-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1839-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1828-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1837-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1827-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1832-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1840-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1830-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1846-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Aug 16, 2022Z-1833-2022—open, classified

Cook Medical identified that devices from the affected device lots may have a complete breach of the chevron seal of the packaging. Therefore, the sterility of affected devices may be compromised.

Jul 19, 2022Z-1718-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Jul 19, 2022Z-1706-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Jul 19, 2022Z-1712-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Jul 19, 2022Z-1715-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Jul 19, 2022Z-1716-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Jul 19, 2022Z-1717-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Jul 19, 2022Z-1714-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Jul 19, 2022Z-1713-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Jul 19, 2022Z-1709-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Jul 19, 2022Z-1708-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Jul 19, 2022Z-1710-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Jul 19, 2022Z-1711-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Jul 19, 2022Z-1707-2022—open, classified

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

May 25, 2022Z-1362-2022—completed

The products may contain excess coating material on the outside and/or interior of the needle component. Potential adverse events that may occur if an affected product is used include a delay in the procedure, a prolonged procedure, or particulate entering the bloodstream which may result in pulmonary embolism or ischemia.

May 5, 2022Z-1240-2022—open, classified

The loading cartridges included with these devices may contain a small, unintended, stainless-steel cannula.

May 5, 2022Z-1242-2022—open, classified

The loading cartridges included with these devices may contain a small, unintended, stainless-steel cannula.

May 5, 2022Z-1241-2022—open, classified

The loading cartridges included with these devices may contain a small, unintended, stainless-steel cannula.