Vidacare Corporation
United StatesFDA applicant, unverified
- Devices
- 21
- FDA recalls
- 2
At a glance
Market reach
- United States
- FDA recalls
What Vidacare Corporation makes
Vidacare Corporation manufactures intraosseous infusion systems, bone access and bone biopsy systems, and bone marrow aspiration systems. Their products include the EZ-CONNECT, THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM, POWERED PD-IO INTRAOSSEOUS INFUSION SYSTEM, VIDAPORT INTRAOSSEOUS INFUSION SYSTEM, PD-IO DISPOSABLE INTRAOSSEOUS INFUSION NEEDLE, THE ONCONTROL BONE ACCESS AND BONE BIOPSY SYSTEM, POWERED EZ-IO PEDIATRIC BONE MARROW ASPIRATION SYSTEM, EZ-MIO DISTAL TIBIA, EZ-IO DISTAL TIBIA, VERTEBRAL ACCESS SYSTEM, EZ-MIO STERNAL, EZ-MIO MANUAL DRIVER, and ONCONTROL BONE MARROW BIOPSY SYSTEM.
The company's portfolio includes Class I and Class II devices, which are listed in the FDA 510(k) registry. Vidacare Corporation is based in the US.
Catalogue
Search and filter all 21 devicesFDA recalls
FDA recall records list 2 recalls initiated by Vidacare Corporation, the earliest on 2014-03-31 and the most recent on 2015-05-12. By recorded status: 2 terminated. The reasons filed fall into these groups: sterility or contamination and manufacturing or quality process. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2015
- 12 May 2015 Z-1801-2015 Class II Terminated Potential breach in sterility
2014
- 31 Mar 2014 Z-2672-2014 Class II Terminated The voluntary recall is due to the needle set not meeting its specifications.
Full distribution text
- 31 Mar 2014 Z-2672-2014 Class II Terminated The voluntary recall is due to the needle set not meeting its specifications.
Frequently asked questions
How many devices does Vidacare Corporation have in the registry?
The registry currently lists 21 devices for Vidacare Corporation. Devices recorded under merged duplicate company entries are counted once.
Which registries list Vidacare Corporation's devices?
Among its 21 most recently registered devices, Vidacare Corporation has devices listed in FDA 510(k) (21 devices).
What risk classes do Vidacare Corporation's devices fall under?
Among its 21 most recently registered devices, the classes recorded for Vidacare Corporation's devices are Class I and Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for Vidacare Corporation?
FDA recall records list 2 recalls initiated by Vidacare Corporation, the most recent initiated on 12 May 2015. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.
What are the newest devices from Vidacare Corporation in the registry?
The most recently registered devices listed for Vidacare Corporation include EZ-IO INTRAOSSEOUS INFUSION SYSTEM, EZ-CONNECT, The OnControl Bone Marrow Biopsy System by Vidacare and THE T.A.L.O.N. INTRAOSSOUS INFUSION SYSTEM BY VIDACRE.