Scientia Vascular, Inc.
Scientia Vascular, Inc. has 3 FDA enforcement events on this register (3 product records) between 2023 and 2025: 3 device; the busiest year was 2025 with 2.
0% of its events are Class I; the most common class is Class II (3). 3 events are listed as ongoing; the recalling firm's address is in UT.
Recall classification reflects the relative degree of health hazard. Event counts depend on a firm's size and product range; they are not a comparison of one firm with another.
Enforcement events
| Initiated | Product (first record) | Type | Class | Records | Status |
|---|---|---|---|---|---|
| 16 Jan 2025 | 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. | Device | Class II | 1 | Ongoing |
| 2 Jan 2025 | Socrates 38 Aspiration Catheter 127 cm length REF SC038-127-001 The Socrates Aspiration System with a compatible suction pump is intended for use in the revascularization of patients with acute ischemic stroke | Device | Class II | 1 | Ongoing |
| 1 Feb 2023 | Plato 17 Microcatheter: Straight Tip, PL17-160-000 ; 45 degree Tip, PL17-160-045; 90 degree Tip, PL17-160-090 | Device | Class II | 1 | Ongoing |
By type and class
Class I: 0% of this firm's events; 18% of all events on the register.
Events by year
Questions and answers
How many FDA recalls has Scientia Vascular, Inc. had?
3 enforcement events (3 product records) on this register, 2023–2025: 3 device.
Are any Scientia Vascular, Inc. recalls ongoing?
3 events are listed as ongoing in the current openFDA export.
What class are Scientia Vascular, Inc. recalls?
3 Class II. 0% are Class I against 18% of all events on the register. Class reflects the relative degree of health hazard of the product, not the firm.
Where does this data come from?
openFDA food, drug and device enforcement reports (CC0), export dated 28 Sep 2026.
Provenance
Source: openFDA enforcement reports (CC0), export dated 28 Sep 2026. Firm names are grouped exactly as FDA spells them; the same company can appear under several spellings. Only organisations are shown. See the methodology.