Recall Z-1690-2016— Becton Dickinson & Company
Class II · Terminated
Class II FDA medical device recall by Becton Dickinson & Company, initiated 2016-03-18, terminated 2017-07-19. FDA's recall record names no specific 510(k) clearance for this event. 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. Reason: The device may have a defect in the catheter. In some instances this defect could result in catheter separation or breakage..
- Recalling firm
- Becton Dickinson & Company
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2016-03-18
- Terminated
- 2017-07-19
- Firm location
- Franklin Lakes, NJ, United States
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
Reason for recall
The device may have a defect in the catheter. In some instances this defect could result in catheter separation or breakage.
Data sourced from openFDA. This site is unofficial and independent of the FDA.