J & J Solutions, Inc. D/B/A/ Corvida Medical
United StatesFDA applicant, unverified
- Devices
- 2
- FDA recalls
- 1
At a glance
Market reach
- United States
- FDA recalls
What J & J Solutions, Inc. D/B/A/ Corvida Medical makes
J & J Solutions, Inc. (Corvida Medical) manufactures sterile connectors and adaptors for intravenous lines, vials, and syringes, including closed-system designs to prevent contamination during medication preparation. Their products include vial adaptors sized for 13mm, 20mm, and 28mm necks, syringe adaptors, and line adaptors intended for hospital pharmacy and clinical use.
The company’s devices are classified as Class II under FDA regulations and are authorised through 510(k) clearance. Their products are listed in the FDA’s 510(k) database, and the manufacturer operates from the United States.
Catalogue
- Regimes: 510(k) Registry: 510(k)
Halo Ref K150486
Regimes: 510(k) Registry: 510(k)
FDA recalls
FDA recall records list 1 recall initiated by J & J Solutions, Inc. D/B/A/ Corvida Medical, initiated on 2016-11-22. By recorded status: 1 terminated. The reasons filed fall into these groups: other reasons as filed. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
2016
- 22 Nov 2016 Z-1003-2017 Class II Terminated Product malfunction: Needle does not retract.
Frequently asked questions
How many devices does J & J Solutions, Inc. D/B/A/ Corvida Medical have in the registry?
The registry currently lists 2 devices for J & J Solutions, Inc. D/B/A/ Corvida Medical. Devices recorded under merged duplicate company entries are counted once.
Which registries list J & J Solutions, Inc. D/B/A/ Corvida Medical's devices?
Among its 2 most recently registered devices, J & J Solutions, Inc. D/B/A/ Corvida Medical has devices listed in FDA 510(k) (2 devices).
What risk classes do J & J Solutions, Inc. D/B/A/ Corvida Medical's devices fall under?
Among its 2 most recently registered devices, the classes recorded for J & J Solutions, Inc. D/B/A/ Corvida Medical's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for J & J Solutions, Inc. D/B/A/ Corvida Medical?
FDA recall records list 1 recall initiated by J & J Solutions, Inc. D/B/A/ Corvida Medical, the most recent initiated on 22 Nov 2016. 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 J & J Solutions, Inc. D/B/A/ Corvida Medical in the registry?
The most recently registered devices listed for J & J Solutions, Inc. D/B/A/ Corvida Medical include Halo Closed Vial Adaptor (Multiple Models based on 13, 20 or 28mm Vial Neck Size), Halo Closed Syringe Adaptor, Halo Closed Line Adaptor, Closed Vial Adaptor and Halo.