Recall Z-0499-2025

Cook Incorporated · initiated October 14, 2024

Class II Open, Classified

Class II – products that might cause a temporary health problem or pose a slight threat of a serious nature

Product

Approach CTO Micro Wire Guide, RPN CMW-14-190-25G, GPN G50789

Codes / lots: UDI-DI: 00827002507890; Lot Numbers: NS15635381 NS15618280 NS15466311 NS15212224 NS14992020

Reason for recall

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

FDA-determined cause: Labeling Change Control

Action taken

An "URGENT: MEDICAL DEVICE RECALL" notification letter dated 10/14/24 was sent to customers. Actions to be Taken by the Customer 1. Examine inventory immediately to determine if you have affected product(s) and quarantine any affected product that remains unused. Immediately cease all further distribution and use of the affected products. 2. Return the affected product(s) to Cook Medical with a copy of the Acknowledgement and Receipt Form to receive a product credit. Refer to the Acknowledgement and Receipt Form for return instructions. 3. Please complete the Acknowledgement and Receipt Form within 5 business days of receiving this letter regardless of whether you have affected product(s) on hand. You may return the Form via fax (812.339.7316) or email (FieldActionsNA@CookMedical.com). 4. This notice must be shared with appropriate personnel, including down to the user level, within your organization or with any organization where the affected devices have been transferred. 5. Please immediately report adverse events to Cook Medical Customer Relations by phone at 800.457.4500 or 812.339.2235, Monday through Friday between 7:30am and 5:00pm (Eastern Time), or by email to: CustomerRelationsNA@CookMedical.com. Action being Taken by Cook Medical Cook Medical is removing affected products from the market. If you have any questions or concerns, please contact Cook Medical Customer Relations at 800.457.4500.

Details

Recall number
Z-0499-2025
Initiated
October 14, 2024
Posted by FDA
November 21, 2024
Product code
DQX – Wire, Guide, Catheter
Quantity
10 units
Distribution
International Distribution to: Korea only
Recalling firm
Cook Incorporated, Bloomington, IN

Official FDA recall record