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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 13 of 194
DeviceModel / ReferenceRegistriesClassStatus
Tornado G10425
FDA UDI
Class IIActive
Zenith G55199
FDA UDI
Class IIIActive
Advance G26887
FDA UDI
Class IIActive
Bander G16997
FDA UDI
UActive
Cook G29553
FDA UDI
Class IIActive
Torcon NB G46967
FDA UDI
Class IIActive
Torcon NB G10910
FDA UDI
Class IIActive
Cook G23553
FDA UDI
Class IIActive
Malecot G14643
FDA UDI
Class IIActive
Cook G06357
FDA UDI
Class IActive
Royal Flush G06535
FDA UDI
Class IIActive
Tornado G11056
FDA UDI
Class IIActive
MReye G20055
FDA UDI
Class IIActive
Amplatz G03304
FDA UDI
Class IIUnknown
Cook Spectrum G20072
FDA UDI
Class IIActive
Cook G04212
FDA UDI
Class IIActive
Ciaglia Blue Rhino G12514
FDA UDI
Class IIActive
Formula 418 G56609
FDA UDI
Class IIIActive
Advance G18960
FDA UDI
Class IIActive
Amplatz G04055
FDA UDI
Class IIActive
Cook G01471
EUDAMEDFDA UDI
Class IIActive
Fuhrman G09700
FDA UDI
Class IActive
Franseen G01305
FDA UDI
Class IActive
Blue Rhino G57690
FDA UDI
Class IIActive
Sof-Flex G15150
FDA UDI
Class IIActive
Performer G10833
FDA UDI
Class IIActive
Turner G04418
FDA UDI
Class IActive
Ultrathane G17131
FDA UDI
Class IIActive
Cook G06261
FDA UDI
Class IIActive
Cook Spectrum G44126
FDA UDI
Class IIActive
Performer G08308
FDA UDI
Class IIActive
Cook G47299
FDA UDI
Class IIUnknown
Torcon NB G05204
FDA UDI
Class IIActive
Cook G04135
FDA UDI
Class IIActive
Zenith Spiral-Z G55218
FDA UDI
Class IIIActive
Performer G10660
FDA UDI
Class IIActive
Cook G03176
FDA UDI
Class IIActive
Coons G04533
FDA UDI
Class IIActive
Cook G00426
FDA UDI
Class IIActive
Cook G35944
FDA UDI
Class IIActive
Cook G02234
FDA UDI
Class IIActive
Cook G02640
FDA UDI
Class IIActive
Cantata G23799
FDA UDI
Class IIActive
Approach G52939
FDA UDI
Class IIActive
Cook G09499
FDA UDI
UActive
Performer G28477
FDA UDI
Class IIActive
Cook G47298
FDA UDI
Class IIActive
Dawson Mueller G27298
FDA UDI
UActive
Malecot G14795
FDA UDI
Class IIActive
Advance G34991
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

Importers

Not available yet.

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.