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Becton Dickinson & Company recalls 1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded IV catheter (0.7 mm x 19 mm) made of FEP polymer catalog number
Recalled May 25, 2016 · FDA recall Z-1690-2016 · Becton Dickinson &
Hazard
The device may have a defect in the catheter. In some instances this defect could result in catheter separation or breakage. · FDA Class II
Units
1,305,150 units
Sold at
Nationwide
Description
The device may have a defect in the catheter. In some instances this defect could result in catheter separation or breakage.
Product
1) 24 G x 0.75 in. BD Angiocath" Autoguard" shielded IV catheter (0.7 mm x 19 mm) made of FEP polymer catalog number 381700 2) 24 G x 0.56 in. BD Angiocath-N" Autoguard" shielded IV catheter (0.7 mm x 14 mm) made of FEP polymer catalog number 381720
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →