FDA Recall Open, Classified

Plato 17 Microcatheter REF PL17-160-090 To assist in delivery of therapeutic devices and embolization materials and infusion of diagnostic agents to the neuro and peripheral vasculature during interventional or diagnostic procedures.

Recall: Z-1235-2025 · Initiated January 16, 2025

Recall

Recall Number
Z-1235-2025
Event Number
96175
Firm
Scientia Vascular, Inc.
FEI Number
3009546466
Product Code
QJP
Status
Open, Classified
Root Cause
Under Investigation by firm
Initiated
January 16, 2025
Posted
February 26, 2025
Address
2460 S 3270 W, West Valley City, UT, 84119-1116

Description

Plato 17 Microcatheter REF PL17-160-090 To assist in delivery of therapeutic devices and embolization materials and infusion of diagnostic agents to the neuro and peripheral vasculature during interventional or diagnostic procedures.

Reason

Due to manufacturing non-conformance that resulted in channels in the seal on the packaging pouch. As a result, this could potential create a breach in the sterile barrier.

Action

On 01/02/2025, the firm email an "URGENT: MEDICAL DEVICE RECALL" Letter to customers informing them that through internal evaluation of finished goods of the Plato 17 Microcatheter, one lot of pouches containing the 90 Tip Plato 17 Microcatheter was identified with pouches that had a gap in the sterile barrier seal. Customer are instructed to: In situations where a device has already been used in a patient procedure, closely monitor patients for signs and symptoms of post-surgical infection. Customer Service will be available to provide additional information and provide replacement orders at [email protected] or (888)385-9016; Monday through Friday, 8:00 AM to 4:30 PM, Mountain Time.

Distribution

U.S. Nationwide distribution in the state of DE.

Quantity

1 unit