FDA Medical Device Recalls (openFDA)
Atrium Medical Corporation: iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616
- Recall number
- Z-0024-2025
- Recalling firm
- Atrium Medical Corporation
- Product
- iCast Covered Stent, 6MMx16MMx120CM, Model Number 42616
- Status
- Open, Classified
- Initiated
- 2024-09-09
- Posted
- 2024-10-07
- Terminated
- not on file
- Reason
- There is an error in the Unique Device Identifier (UDI) printed on the product's distribution label.
- Root cause
- Under Investigation by firm
- Action
- 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.
- Quantity
- 11 devices
- Distribution
- US Nationwide distribution in the states of FL, MA, MI, OH, WA.
- Lot, serial or model codes
- UDI-DI: 00650862426168; Lot Number: 508083; Serial Numbers: 508083031, 508083032, 508083034, 508083035, 508083036, 508083037, 508083038, 508083039, 508083040, 508083041, 508083042
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- PRL
- Firm FEI
- 3011175548
- Firm city
- Merrimack
- Firm state
- NH
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28