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 381
FDA device recall Z-1690-2016 · posted 2016-05-18 · Terminated
Recall details
- Recalling firm
- Becton Dickinson & Company
- Reason for recall
- The device may have a defect in the catheter. In some instances this defect could result in catheter separation or breakage.
- Action taken
- BD isssued an urgent voluntary product recall lettter/recall response card on 3/18/2016.
- Root cause
- Device Design
- Status
- Terminated
- Product code
- FOZ
- Quantity affected
- 1,305,150 units
- Distribution
- Nationwide
- Date initiated
- 2016-03-18
- Date posted
- 2016-05-18
- Date terminated
- 2017-07-19
- Location
- Franklin Lakes, NJ
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