RecallRadar

FDA Device recall Z-2468-2021

BD SmartSite Bag Access Device Needle-Free Valve, REF: 2300E

On 2021-09-22 the FDA classified a Class II recall of BD SmartSite Bag Access Device Needle-Free Valve, REF: 2300E by Carefusion, citing needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which c….

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-2468-2021
ClassificationClass II
Statusongoing
Initiated2021-08-02
Published2021-09-22
Last updated2026-09-13 11:56 UTC
CompanyCarefusion
DistributionUS

Product

BD SmartSite Bag Access Device Needle-Free Valve, REF: 2300E; BD Bag access Device with 1 Check Valve And Needle Free Valve, REF: 2309E-0006

Reason

Needle-free connector valves, either standalone or attached to extension sets, may have issues including difficulty to flush, flow issues, and partial or total occlusions, which could lead to therapy delay. Follow-up activates not required if product has already been used or was safely connected to the female luer of connecting device.

Identifiers

code_info
Lots: 20066502 20066503 20066504 20076251 20076352 20086483 20086484 20086485 20086486 20087129 20087130 2…Lots: 20066502 20066503 20066504 20076251 20076352 20086483 20086484 20086485 20086486 20087129 20087130 20096280 20096281 20096282 20096283 20097163 20105074 20105075 20095374 20095375 20096302 20105754 20105755 20105756 20105757 20105758 20115470 21036462 21036463 21036464 21036465 21036466

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:56 UTC. Current status: ongoing.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2468-2021%22

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