Reported Sep 22, 2021 · Ongoing
BD SmartSite Bag Access Device Needle-Free Valve, REF: 2300E; BD Bag access Device with 1 Check Valve And Needle Free…
Carefusion
Moderate riskThis product could cause temporary or reversible health problems — stop using it.What you should do
Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.
Firm contact: CAREFUSION · 10020 Pacific Mesa Blvd · San Diego, CA · 92121-4386
Is this the product you have?
- BD SmartSite Bag Access Device Needle-Free Valve
- REF2300E; BD Bag access Device with 1 Check Valve And Needle Free Valve
- REF2309E-0006
- Lot codes and dates
- Lots
2006650220066503200665042007625120076352200864832008648420086485200864862008712920087130200962802009628120096282200962832009716320105074201050752009537420095375200963022010575420105755201057562010575720105758201154702103646221036463210364642103646521036466
- Lots
- Amount recalled
- 295,331
This recall covers 15 products
The agency filed one notice per product. You are reading one of them; the other 14 are below.
2 more are in the archive.
Where it was sold
Why it was recalled
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.
This product could cause temporary or reversible health problems — stop using it.
Want the full recall guide?
The guide adds the identifying codes laid out for scanning, symptoms to watch for, a timeline, and news coverage of this recall.
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