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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 3 of 194
DeviceModel / ReferenceRegistriesClassStatus
Blue Rhino G57689
FDA UDI
Class IIActive
Memory Basket G21552
FDA UDI
Class IIUnknown
Pigtail G14157
FDA UDI
Class IIActive
Torcon NB G47092
FDA UDI
Class IIActive
Flexor G19174
FDA UDI
Class IIActive
Torcon NB G04789
FDA UDI
Class IIActive
Newton G01140
FDA UDI
Class IIActive
Cook G00071
FDA UDI
Class IIActive
Cook-Cope Loop G14658
FDA UDI
Class IIActive
Quantum TTC G22766
FDA UDI
Class IIActive
Royal Flush G12698
FDA UDI
Class IIActive
Torcon NB G07268
FDA UDI
Class IIActive
Amplatz G14485
FDA UDI
Class IIActive
Fusion G31530
FDA UDI
Class IIUnknown
Cook G03265
FDA UDI
Class IIActive
Bander G16996
FDA UDI
UActive
Cook G16699
FDA UDI
Class IIActive
Cook G00363
FDA UDI
Class IIActive
Amplatz G11684
FDA UDI
Class IIActive
Cook G06338
FDA UDI
Class IActive
Cook G04378
FDA UDI
Class IActive
Micropuncture G47951
FDA UDI
Class IIActive
Vital-Port G26432
FDA UDI
Class IIActive
Flexi-Tip G14809
FDA UDI
Class IIActive
Performer G08434
FDA UDI
Class IIActive
Torcon NB G08078
FDA UDI
Class IIActive
Zenith Flex G48451
FDA UDI
Class IIIUnknown
Cook G00983
EUDAMEDFDA UDI
Class IIActive
Flexor G19177
FDA UDI
Class IIActive
Zenith G12484
FDA UDI
Class IIIActive
Tenckhoff G08994
FDA UDI
Class IActive
Check-Flo G06002
FDA UDI
Class IIActive
Cook G02260
FDA UDI
Class IIActive
Cook G09829
FDA UDI
UActive
Williams G14220
FDA UDI
Class IIActive
Cook G14042
FDA UDI
Class IIActive
Cook G01617
FDA UDI
Class IActive
Cook Spectrum G24716
FDA UDI
Class IIActive
Peel-Away G06580
FDA UDI
Class IIActive
Malecot G14454
FDA UDI
UActive
Cook G14276
FDA UDI
Class IIActive
Royal Flush G05188
FDA UDI
Class IIActive
Peel-Away G04386
FDA UDI
Class IIUnknown
Torcon NB G09757
FDA UDI
Class IIActive
Cook G46199
FDA UDI
Class IIActive
Cook G02672
FDA UDI
Class IIActive
Ciaglia Blue Rhino G13166
FDA UDI
Class IIUnknown
Dolphin BT G36106
FDA UDI
Class IIActive
Saeed G25503
FDA UDI
Class IIUnknown
Beacon Tip Torcon NB G11726
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.