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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 6 of 194
DeviceModel / ReferenceRegistriesClassStatus
Cook G07214
FDA UDI
Class IIActive
HiWire G30473
FDA UDI
Class IIActive
Franseen G02529
FDA UDI
Class IActive
Zenith Flex G48419
FDA UDI
Class IIIActive
Cook G58819
FDA UDI
Class IIActive
Cook G00273
FDA UDI
Class IIActive
Cook G00552
FDA UDI
Class IIActive
Cook G00662
FDA UDI
Class IIActive
Newton G00573
FDA UDI
Class IIActive
Slip-Cath Beacon Tip G31333
FDA UDI
Class IIActive
Cook G10047
FDA UDI
Class IIActive
Entuit G35569
FDA UDI
Class IIActive
Formula 418 G42936
FDA UDI
Class IIActive
Cook G57483
FDA UDI
Class IIActive
Flexor G11633
FDA UDI
Class IIActive
Cook G00674
FDA UDI
Class IIActive
Cook G01654
FDA UDI
Class IIUnknown
Royal Flush G12137
FDA UDI
Class IIActive
Torcon NB G46949
FDA UDI
Class IIActive
Slip-Cath Beacon Tip G31326
FDA UDI
Class IIActive
Cook G14114
FDA UDI
Class IActive
Cook G04224
FDA UDI
Class IIActive
Peel-Away G05513
FDA UDI
Class IIActive
Amplatz G17976
FDA UDI
Class IIActive
Peel-Away G08799
FDA UDI
Class IIActive
Cook G10049
FDA UDI
UActive
Tornado G13209
FDA UDI
Class IIActive
Flexor G11605
FDA UDI
Class IIActive
Cook G10714
FDA UDI
Class IActive
Schwarz G03408
FDA UDI
Class IIActive
Universa G49873
FDA UDI
Class IIActive
Cook Spectrum G43984
FDA UDI
Class IIActive
Cook G16987
FDA UDI
Class IIActive
Amplatz G17967
FDA UDI
Class IIActive
Blue Rhino G57684
FDA UDI
Class IIActive
Cook G58842
FDA UDI
Class IIActive
Cor-Flex G03603
FDA UDI
Class IIActive
Cook G01117
FDA UDI
Class IIActive
Cook G07966
FDA UDI
Class IIActive
Tornado G11054
FDA UDI
Class IIActive
Advance G31211
FDA UDI
Class IIActive
Rosen G03889
FDA UDI
Class IIUnknown
MReye G47924
FDA UDI
Class IIActive
Optilite G48616
FDA UDI
Class IIActive
Hercules G35269
FDA UDI
Class IActive
Shepard G16469
FDA UDI
Class IIActive
Universa G53691
FDA UDI
Class IIActive
Cook G25981
FDA UDI
Class IIActive
Cook G10501
FDA UDI
Class IActive
Cook Spectrum Turbo-Ject G18234
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

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.