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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 14 of 194
DeviceModel / ReferenceRegistriesClassStatus
Zenith Flex G48428
FDA UDI
Class IIIActive
Cook G26927
FDA UDI
Class IIActive
Zenith Renu G55374
FDA UDI
Class IIIActive
Zenith Flex G48424
FDA UDI
Class IIIActive
Amplatz G04003
FDA UDI
Class IIActive
Quick-Core G10083
FDA UDI
Class IIActive
Cook G01084
FDA UDI
Class IIActive
Beacon Tip Torcon NB G11380
FDA UDI
Class IIActive
Cook Spectrum G49803
FDA UDI
Class IIActive
Nester G47398
FDA UDI
Class IIActive
Melker G47665
FDA UDI
Class IIActive
Tornado G13106
FDA UDI
Class IIActive
Cook G58408
FDA UDI
Class IIActive
Cook G06299
FDA UDI
Class IActive
Torcon NB G04784
FDA UDI
Class IIActive
Malecot G14763
FDA UDI
Class IIActive
Cook G17258
FDA UDI
Class IIActive
Cook G07279
FDA UDI
Class IIUnknown
Ciaglia Blue Rhino G2 G34276
FDA UDI
Class IIActive
Advance G18802
FDA UDI
Class IIActive
Zenith Flex G48404
FDA UDI
Class IIIActive
Zenith Renu G36180
FDA UDI
Class IIIActive
Alight G25427
FDA UDI
Class IIUnknown
Cook G00415
FDA UDI
Class IIUnknown
Universa G23469
FDA UDI
Class IIActive
Peel-Away G02103
FDA UDI
Class IIUnknown
Cook G00043
FDA UDI
Class IIActive
Retracta G34187
FDA UDI
Class IIActive
Kwart G14836
FDA UDI
Class IIActive
Ring G06728
FDA UDI
UActive
Beacon Tip Torcon NB G08641
FDA UDI
Class IIActive
Coons-Bentson G15591
FDA UDI
Class IIUnknown
Cook G06358
FDA UDI
Class IActive
Cook G24764
FDA UDI
Class IIActive
Performer G09439
FDA UDI
Class IIActive
Cook G07835
FDA UDI
Class IIUnknown
Cook G51534
FDA UDI
Class IIActive
Cook Spectrum G51267
FDA UDI
Class IIActive
Cook Spectrum G50821
FDA UDI
Class IIActive
Torcon NB G47030
FDA UDI
Class IIActive
Captura G31576
FDA UDI
Class IIActive
Cxi G52544
FDA UDI
Class IIActive
Cook G27280
FDA UDI
Class IIActive
Pigtail G14152
FDA UDI
Class IIActive
Flexor G46076
FDA UDI
Class IIActive
LapSac G16495
FDA UDI
Class IActive
HiWire G36275
FDA UDI
Class IIActive
Cook G17653
FDA UDI
Class IActive
Micropuncture G08654
FDA UDI
Class IIActive
Cook G08387
FDA UDI
Class IIActive

Related Companies

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Importers

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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.