Recall Z-0024-2025

Atrium Medical Corporation · initiated September 9, 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

iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616

Codes / lots: UDI-DI: 00650862426168; Lot Number: 508083; Serial Numbers: 508083031, 508083032, 508083034, 508083035, 508083036, 508083037, 508083038, 508083039, 508083040, 508083041, 508083042

Reason for recall

There is an error in the Unique Device Identifier (UDI) printed on the product's distribution label.

FDA-determined cause: Under Investigation by firm

Action taken

An Urgent Medical Device Removal notification letter dated 9/9/24 was sent to customers. Actions to be taken by the Customer: Our records indicate that you have received one or more of the iCast Covered Stents from the affected Product REF and Serial Numbers. Please examine your inventory immediately to determine if you have any of the iCast Covered Stents with the Product REF and Serial Numbers listed in this notice, which can be found on the product label. " Should you have any affected product, do not use the product and remove it from areas of use. " Please forward this information to all current and potential iCast Covered Stent System users within your hospital/ facility. " If you are a distributor who has shipped any affected product(s) to customers, please forward this document to their attention for appropriate action. " Please contact your local Atrium Medical Corporation/Getinge Customer Support department at (888) 943-8872 (press option 2), Monday through Friday, between the hours of 8:00 a.m. and 6:00 p.m. (Eastern Time Zone) to receive instructions for returning any affected unused product within expiry per the iCast label. You will receive credit upon the return of any affected devices. " Whether or not you have affected product(s) with the Product REF number and Serial Numbers listed in this notice, please complete and sign the attached MEDICAL DEVICE - REMOVAL RESPONSE FORM to acknowledge that you have received this notification. Return the completed form to Getinge by emailing a scanned copy to trium.icastcooklabel.act@getinge.com. Type of Action by Atrium Medical Corporation/Getinge: If requested, Atrium Medical Corporation/Getinge will facilitate the removal of affected products from your facility and provide credit for your return of these products. If you have any questions, please call Atrium Medical Corporation/Getinge Customer Support at (888) 943-8872 (press option 2), Monday through Friday, between the hours of 8:00 a.m. and 6:00 p.m.

Details

Recall number
Z-0024-2025
Initiated
September 9, 2024
Posted by FDA
October 7, 2024
Product code
PRL – Iliac Covered Stent, Arterial
Quantity
11 devices
Distribution
US Nationwide distribution in the states of FL, MA, MI, OH, WA.
Recalling firm
Atrium Medical Corporation, Merrimack, NH

Official FDA recall record