International Medical Devices Database

Manufacturer Address
Us Endovascular, 1150 Milwaukee St, Saint Louis MO 63122-7336
Manufacturer Parent Company (2017)
Steris Plc
Source
USFDA
1 Event
- Recall of Device Recall USE PTA 0.014 RX Catheter

One device in the database

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 1717082810164810 1717101610166290 1717101610166290 1717101610166290 1717082810164810 1717082810164810 1717101610166290 1717101610166290 1717101610166290 1717101610166290 1717082810164810 1717101610166290 1717082810164810 1717082810164810 1717082810164810 1717082810164810 1717082810164820 1717082810164820 1717101610166300 1717082810164820 1717101610166300 1717101610166300 1717082810164820 1717101610166300 1717082810164820 1717101610166300 1717082810164820 1717082810164820 1717082810164820 1717101610166300 1717101610166310 1717101610166310 1717101610166310 1717082810164850 1717082810164850 1717101610166320 1717101610166320 1717101610166320 1717101610166320 1717101610166320 1717101610166320 1717101610166320 1717082810164850 1717082810164850 1717082810164860 1717101610166330 1717101610166330 1717101610166330 1717101610166330 1717101610166340 1717101610166340 1717101610166340 1717101610166340 1717101610166340 1717101610166340 1717082810164890 1717082810164890 1717082810164890 1717101610166350 1717101610166350 1717101610166350 1717101610166350 1717101610166350 1717082810164890 1717101610166350 1717101610166350 1717082810164890 1717101610166350 1717101610166350 1717101610166350 1717101610166350 1717101610166350 1717082810164890 1717082810164890 1717082810164900 1717082810164900 1717101610166360 1717101610166360 1717101610166360 1717101610166360 1717101610166360 1717101610166360 1717101610166360 1717101610166360 1717101610166360 1717101610166360 1717082810164750 1717082810164750 1717082810164750 1717082810164750 1717082810164750 1717082810164750 1717082810164750 1717082810164750 1717082810164750 1717082810164750 1717082810164750 1718041510177210 1718010810171540 1718010810171540 1718010810171540 1718010810171540 1718010810171540 1718010810171540 1718010810171540 1718010810171540 1718010810174410 1718010810174410 1718010810171540 1718051310179200 1718010810171550 1718010810171550 1718010810171550 1718010810171550 1718010810171550 1718010810171550 1718010810171550 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1717082810164790 1718041510177230 1718051310179210 1718051310179210 1718051310179210 1718051310179210 1718041510177240 1718041510177240 1718041510177240 1718041510177240 1718041510177240 1718051310179220 1718041510177240 1718041510177240 1718041510177240 1718051310179220 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1717082810164830 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718010810171560 1718051310179230 1718051310179230 1718051310179230 1718010810171570 1718010810171570 1718010810171570 1718010810171570 1718010810171570 1718010810171570 1718010810171570 1718010810171570 1718010810171570 1718010810171570 1718051310179240 1718051310179240 1718051310179240 1718051310179240 1718010810171570 1717082810164870 1717082810164870 1717082810164870 1717082810164870 1717101610169170 1717101610169170 1717101610169170 1717101610169170 1717082810164870 1717082810164870 1718071310185370 1718051310179250 1718051310179250 1718051310179250 1718051310179250 1718051310179250 1718051310179260 1718051310179260 1717082810164910 1717082810164910 1717082810164910 1717101610167680 1717101610167680 1717101610167680 1717101610167680 1717101610167680 1717101610167680 1717082810164910 1717101610167680 1717101610167680 1717101610167680 1717101610167680 1717101610167680 1717101610167680 1717101610167680 1717101610167680 1717101610167680 1718061710181860 1718061710181860 1718061710181860 1718041510177250 1718041510177250 1718061710181900 1718061710181900 1718061710181900 1718061710181900 1718061710181900
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.

8 manufacturers with a similar name

Learn more about the data here

Micrus Endovascular Corp

Manufacturer Parent Company (2017)
Johnson & Johnson
Source
NZMMDSA

Micrus Endovascular

Manufacturer Parent Company (2017)
Johnson & Johnson
Source
LAANSM

Micrus Endovascular Corp.

Manufacturer Parent Company (2017)
Johnson & Johnson
Source
BAM

Micrus Endovascular

Manufacturer Parent Company (2017)
Johnson & Johnson
Source
SATP

3 more

About this database

Explore more than 120,000 Recalls, Safety Alerts and Field Safety Notices of medical devices and their connections with their manufacturers.

Stories in your inbox

Do you work in the medical industry? Or have experience with a medical device? Our reporting is not done yet. We want to hear from you.

Tell us your story!

Disclaimer

Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

Download the data

The International Medical Devices Database is licensed under the Open Database License and its contents under Creative Commons Attribution-ShareAlike license. Always cite the International Consortium of Investigative Journalists when using this data. You can download a raw copy of the database here.

Download all (zipped)

Us Endovascular

One device in the database

Device Recall USE PTA 0.014 RX Catheter

8 manufacturers with a similar name

Micrus Endovascular Corp

Micrus Endovascular

Micrus Endovascular Corp.

Micrus Endovascular

Micrus Endovascular