Recall Z-1991-2024 ยท DSY Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
Atrium Medical Corporation
ADVANTA VXT, 6X100, 1GDS, FH, STR-TW. Single-Ended Slider GDS. Vascular graft
| Date | Jun 4, 2024 (initiated May 3, 2024) |
| Status | Open, Classified |
| Reason | Complaints of reported separation of the Slider GDS Swivel Rod from the Swivel Core and of a notable gap between the two pieces. |
| Root cause | Equipment maintenance |
| Action | Consignees were sent an URGENT MEDICAL DEVICE- REMOVAL notification by mail, dated 5/3/24. Consignees are instructed to examine their inventory immediately to determine if any recalled product is in their possession. Recalled product possesses the REF number on device labeling and has an expiration date prior to 24FEB2027. All consignees are asked to complete and return the provided response form by email to GDSgrafts2024@getinge.com or by fax to 1-866-560-4062. Consignees that are distributors are asked to forward the provided notification to their customers. Consignees are to post a copy of |
| Quantity | 53,308 units (US: 11, 236; OUS: 42,072) |
| Distribution | 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, CZ, DE, DZ, EC, EE, EG, ES, FI, FR, GB, GR, HK, ID, IE, IL, IQ, IT, JO, JP, KR, KW, LT, LU, LV, ME, MN, MU, MX, MY, NI, NL, NO, NZ, OM, PA, PE, PH, PK, PL, PT, P |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K992960 | ADVANTA GRAFT (>6MM) Atrium Medical Corp., Oct 1, 1999 |