FDAJune 20, 2022device
Intraosseous needle and driver. Catalog/Device Name: D015151NK/BD Needle Kit for Powered Driver 15mm x 15Ga, D015151MK/ BD Manual Driver Needle Kit 15mm x 15Ga, D015251NK/ BD Needle Kit for Powered Driver 25mm x 15Ga, D015251MK/ BD Manual Driver Needle Kit 25mm x 15Ga, D015351NK/ BD Needle Kit fo...
Official recall recorded by the U.S. Food & Drug Administration.
The hazard
BD Intraosseous Needle Kits may exhibit: 1) Increased force required to remove the stylet from intraosseous needle during placement may cause removal of the entire needle assembly and loss of intraosseous access; 2) Stylet safety mechanism may not engage as the stylet is removed; 3) Metal discs in the powered driver may stick rendering the driver unusable.
What to do
FDA enforcement status: Ongoing
Brands named
bard access systemsbardbard access
UPCs
80174116358680174116362380174116367880174116363080174116359380174116364780174116360980174116365480174116361680174116366100801741163579
Recall history
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