Devices

Device Recall USE PTA 0.014 RX Catheter

Model / Serial
All references USE .014RX. Lot numbers: 1717082810164720 1717082810164720 1717082810164720 1717082810164720 1717082810164720 1717082810164730 1717101610166230 1717101610166230 1717101610166230 1717101610166230 1717101610166230 1717101610166230 1717101610166230 1717101610166230 1717101610166230 1717101610166230 1717101610166230 1717101610166230 1717101610166250 1717101610166250 1717082810164740 1717101610166250 1717101610166250 1717082810164740 1717101610166250 1717101610166250 1717082810164760 1717101610166240 1717082810164760 1717082810164770 1717082810164770 1717101610166260 1717101610169180 1717101610169180 1717101610169180 1717101610166260 1717101610169180 1717101610166260 1717082810164770 1717101610166260 1718041510177220 1717082810164770 1717101610169180 1717082810164780 1717101610166270 1717082810164780 1717101610166270 1717101610166270 1717101610169190 1717082810164800 1717101610169190 1717101610169190 1717101610169190 1717101610166280 1717082810164810 1717082810164810 1717101610166290 1717082810164810 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Product Classification
Cardiovascular Devices
Device Class
2
Implanted device?
No
Distribution
US Distribution to the states of : AR, CA, FL, LA, MO, MI, MS, NY, TN, and TX.
Product Description
USE (Ebony) PTA .014" rapid exchange (RX) Peripheral Dilatation Catheter. Distributed by US Endovascular, St. Louis, MO.
Manufacturer
Us Endovascular
1 Event
- Recall of Device Recall USE PTA 0.014 RX Catheter

Manufacturer

Us Endovascular

Manufacturer Address
Us Endovascular, 1150 Milwaukee St, Saint Louis MO 63122-7336
Manufacturer Parent Company (2017)
Steris Plc
Source
USFDA

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