Reported Sep 22, 2021 · Ongoing

BD Alaris Pump Infusion Buerette Set 0.2 Micron Filter Smallbore Tubing SmartSite Port (Burette) SmartSite Y-Site, REF:…

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?

10 of 10 products

Products covered by this recall
Model / numberProduct as published
10015012BD Alaris Pump Infusion Buerette Set 0.2 Micron Filter Smallbore Tubing SmartSite Port (Burette) SmartSite Y-Site
10817920BD Alaris Pump Infusion Buerette Set Ball Valve Smallbore Tubing Smartsite Port (Burette) SmartSite Y-Site
10821753BD Alaris Pump Infusion Buerette Set SmartSite Port (Burette) 3 SmartSite Y-Sites
11607787BD Alaris Pump Infusion Buerette Smallbore Tubing Smartsite Port (Burette) SmartSite Y-Site
11613191BD Alaris Pump Infusion Buerette Set 0.2Micron Filter Ball Valve SmartSite Port (Burette) 2 SmartSite Y-Sites
2440-0600BD Alaris Pump Infusion Buerette Set Smartsite Port (Burette) 3 SmartSite Y-Sites
2441-0007BD Alaris Pump Infusion Buerette Set Smallbore Tubing Smartsite Port (Burette) 3 SmartSite Y-Site
2444-0007BD Alaris Pump Infusion Buerette Set Low Sorbing Tubing Smartsite Port (Burette)
2447-0007BD Alaris Pump Infusion Buerette Set Ball Valve Smartsite Port (Burette) 2 Smartsite Y-Sites
C24104EBD Alaris Pump Infusion Set Back Check Valve 4-Way Stopcock 3 Smartsite Y-Sites Extension Set With SmartSite Port
Lot codes and dates
  • Lots

    158 of 158 codes

    • 20055717
    • 20066810
    • 20066818
    • 20066819
    • 20077318
    • 20077321
    • 20077322
    • 20077522
    • 20077523
    • 20077541
    • 20086584
    • 20106957
    • 20106958
    • 20106959
    • 21025085
    • 21025086
    • 21025220
    • 20025114
    • 20025123
    • 20026226
    • 20026227
    • 20026322
    • 20026323
    • 20026382
    • 20026383
    • 20026510
    • 20056946
    • 20056947
    • 20057055
    • 20057056
    • 20017423
    • 20096285
    • 20096286
    • 20015347
    • 20016918
    • 20016919
    • 20016960
    • 20016961
    • 20017112
    • 20035102
    • 20035133
    • 20035134
    • 20035281
    • 20035295
    • 20035296
    • 20035368
    • 20035526
    • 20035527
    • 20035603
    • 20035604
    • 20056757
    • 20065191
    • 20065192
    • 20065281
    • 20065282
    • 20065298
    • 20065299
    • 20065346
    • 20065347
    • 20065362
Amount recalled
344,300

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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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA device enforcement) notice

Data as of Sep 19, 5:43 PM UTC

RecallNow is not a government agency. Every fact on this page is published by the FDA, USDA or CPSC and links back to their notice.