Atrium Medical Corporation 2024-06-12 Health serious FDA
Health · FDA · Recall #FDA-Z-1986-2024
ADVANTA VXT, 6X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft Recall
Issued June 12, 2024 · Atrium Medical Corporation
In June 2024, Atrium Medical Corporation recalled the ADVANTA VXT, 6X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces.
What you should do
- 1 Stop using ADVANTA VXT, 6X70, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Atrium Medical Corporation to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Atrium Medical Corporation
- Category
- Health
- Recall date
- June 12, 2024
- Units affected
- Not reported
- Sold at
- Worldwide distribution - US Nationwide including Puerto Rico, and the countries of AE, AR, AT, AU, BE, BG, BO, BR, CA, CH, CL, CN, CO, CY, C
- Recall number
- FDA-Z-1986-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Atrium Medical Corporation has 9 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.