Recall Z-1989-2025 ยท KRD Device, Vascular, For Promoting Embolization
BALT USA, LLC
Prestige Coil System REFs/UDI-DI codes: PRES0153CXPPLT 00810068567311 PRES1045CPKPLT 00810068567663 PRES1245CPKPLT 00810068567694 PRES1445CPKPLT 00810068567724 PRES0103CXPPLT 00810068567304 PRES2512CXPPLT 00810068567397 PRES0258CXPPLT 00810068567380 PRES0212CXPPLT 00810068567373 PRES0204CXPPLT 00810068567342 PRES0206CXPPLT 00810068567359 PRES0208CXPPLT 00810068567366 PRES3520CXPPLT 00810068567441
| Date | Jun 18, 2025 (initiated May 8, 2025) |
| Status | Open, Classified |
| Reason | Due to radiopaque (RO) marker was not visible during angiography and it was determined that the RO marker was not manufactured to specification. |
| Root cause | Vendor change control |
| Action | On 05/08/2025, the firm sent via priority mail and an, "URGENT: MEDICAL DEVICE RECALL" Letter informing customers that defect impacting specific lots of the Optima and Prestige Coil Systems, in which the distal 3 cm radiopaque (RO) marker may not be visible under fluoroscopy. Customers are instructed to: As a voluntary alternative to returning the affected products, devices from the affected lots can be inspected by trained hospital personnel for the presence of the RO marker using available fluoroscopy imaging equipment prior to a clinical procedure. It is important to conduct this inspectio |
| Quantity | 1754 devices |
| Distribution | Worldwide - U.S. Nationwide distribution including in the states of AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IL, IN, KS, KY, MA, ME, MN, MO, MS, NC, ND, NE, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, VT, WA and WI. The countries of Argentina, Armenia, Australia, Belgium, Brazil, Bulgaria |
| FDA record | Open on fda.gov |
510(k) clearances named in this recall
| K220699 | Prestige Coil System Bait USA, LLC, Apr 8, 2022 |