FDA Recall Open, Classified

Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090

Recall: Z-1249-2023 · Initiated February 1, 2023

Recall

Recall Number
Z-1249-2023
Event Number
91676
Firm
Scientia Vascular, Inc.
FEI Number
3009546466
Product Code
DQY
Status
Open, Classified
Root Cause
Device Design
Initiated
February 1, 2023
Posted
March 13, 2023
Address
2460 S 3270 W, West Valley City, UT, 84119-1116

Description

Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090

Reason

Microcatheters for embolic coil and diagnostic agent introduction to peripheral/neuro vasculature, due to manufacturing non-conformance, and due to flush, guidewire insertion and manipulation prior to placement, may have loose particles within catheter lumens that may be introduced to patients, which could cause embolic event, small vessel occlusion, and subacute to chronic inflammatory response.

Action

On 02/01/23, recall notices were mailed and emailed to customers who were told the following: Actions for Customer/User: Identify and segregate affected devices. Actions for Recalling Firm: Sales representatives will visit and assist with completing the acknowledgement and receipt form and the collection of affected devices. If devices have been transferred from one facility to another the additional consignees will be contacted upon identification. Sales reps received the recall notice and a response form they would take to customers to obtain additional information and the affected devices. Customers with questions can contact customer support at 1-888-385-9016 9016 between the hours of 9:30 AM and 6:30 PM ET (7:30 AM and 4:30 PM MST), Monday through Friday, or via email to [email protected]

Distribution

US Nationwide distribution in the states of IL, AL, FL, NC, WI, GA, SC, IN, KS, CA, OH, NY, NH, CO, MA, NV, UT, TX.

Quantity

353