International Medsurg Connection Hypodermic Needle, 21 G X 1.5 in YALE DISP, 100 per box, 50 recall — FDA Z-2813-2017
Insufficient documentation to support product sterility claims.
Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.
The newest recall records with useful source details are listed here.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Identification of excess plastic on the tip of the cannula.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Insufficient documentation to support product sterility claims.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
Browse recent months with enough recall history for useful comparison.