J&J Solutions, Inc. DBA Corvida Medical

FDA Regulatory Profile

J&J Solutions, Inc. DBA Corvida Medical appears in FDA public data with 1 recall, 0 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (Z-1003-2017, Class II) was initiated on November 22, 2016.

Summary

Total Recalls
1
510(k) Clearances
0
Inspections
0
Compliance Actions
0

Known Names

j and j solutions, inc. dba corvida medical, j and j solutions, inc. d/b/a/ corvida medical

Recent Recalls

NumberClassProductDate
Z-1003-2017Class IIHalo Closed System Transfer Device, closed syringe adaptor, REF CSA100, Rx only, Sterile, packaged aNovember 22, 2016