Reported Sep 22, 2021 · Ongoing

BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV, REF: 10037031; BD Gravity…

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?

6 of 6 products

Products covered by this recall
Model / numberProduct as published
10037031BD Gravity Burette Set 60 DROP 1.2 MF 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV
10037032BD Gravity Burette Set 20 DROP 1.2 Micron Filter 2 SmartSite VALVES BALL VALVE DRIP CHAMBER V/NV
82104EBD GRAVITY BURETTE SET 60 DROP 2 Smartsite VALVES BALL DRIP CHAMBER \VENTED/NONVENTED
82113EBD ADD-ON BURETTE SET Smartsite VALVE
82114EBD ADD-ON BURETTE SET Smartsite VALVE VENTED/NONVENTED
82115EBD ADD-ON BURETTE SET Smartsite VALVE BALL VALVE DRIP CHAMBER VENTED/NONVENTED
Lot codes and dates
  • Lots
    • 20065590
    • 20065591
    • 20075066
    • 20105945
    • 20105946
    • 20105947
    • 20106408
    • 21015533
    • 21015552
    • 20106612
    • 20115540
    • 21046676
    • 20096121
    • 20115539
    • 21025938
    • 21025939
    • 21025940
    • 21025941
    • 21035175
    • 21035176
    • 20066404
    • 21035174
    • 20096120
    • 20106171
    • 20106172
    • 20106173
    • 20106174
    • 20106175
Amount recalled
77,802

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.

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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, 7:40 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.