Devices

Device Recall BD Angiocath Autoguard shielded IV catheter

Model / Serial
Catalog Number 381720 - 24 G x 0.75 in. BD Angiocath" Autoguard" shielded IV catheter (0.7 mm x 19 mm) made of FEP polymer. 3121951 3143801 3190895 3254585 3303872 4051735 4133600 4177944 4219570 4289603 4317642 5063833 5106687 5125665 5230884 5300771 24 G x 0.56 in. BD Angiocath-N" Autoguard" shielded IV catheter (0.7 mm x 14 mm) made of FEP polymer 3045792 3106688 3289840 4059581 4203557 5002915 5063827 5125565 5300772
Product Classification
General Hospital and Personal Use Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide
Product Description
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
Becton Dickinson & Company
1 Event
- Recall of Device Recall BD Angiocath Autoguard shielded IV catheter

Manufacturer

Becton Dickinson & Company

Manufacturer Address
Becton Dickinson & Company, 1 Becton Dr, Franklin Lakes NJ 07417-1815
Manufacturer Parent Company (2017)
Becton, Dickinson and Company
Source
USFDA

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