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Terminated

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

FDA Recall Z-1690-2016 · Posted 2016-05-18

Recalling FirmBecton Dickinson & Company
Recall StatusTerminated
Product CodeFOZ
Date Initiated2016-03-18
Date Terminated2017-07-19
Product Quantity1,305,150 units

Reason for Recall

The device may have a defect in the catheter. In some instances this defect could result in catheter separation or breakage.

Firm Action

BD isssued an urgent voluntary product recall lettter/recall response card on 3/18/2016.

Root Cause

Device Design

Distribution Pattern

Nationwide

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

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