International Medsurg Connection Hypodermic Needle, 22 G X 1.0 in REG BEVEL, 100 per box, 50 recall — FDA Z-2814-2017
Insufficient documentation to support product sterility claims.
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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.
Devices are not consistent with Quality System Requirements.
Devices are not consistent with Quality System Requirements.
There have been five reports of graft thrombosis/occlusion during global commercial use, each following treatment for BTAI. One case resulted in patient death, and three cases resulted in…
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.
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.
Devices are not consistent with Quality System Requirements.
Browse recent months with enough recall history for useful comparison.