Bard recalls NG Sump Tubes with ENFit connectors due to reported inadequate suction and drainage. Affected models include EN0042180 with specific serial numbers. Consumers should check their tubes and contact Bard for details.
BD (C.R. Bard) has received user complaints reporting that during use of BD Bard NG Sump Tubes with ENFit Connectors, inadequate or reduced suction, decompression, and drainage occurred.
Bard is recalling certain nasogastric sump tubes with ENFit connectors because users report they don't drain stomach contents properly. This could lead to fluid buildup or complications if the tube isn't working correctly.
The tubes may not create enough suction to drain stomach contents effectively. This can cause fluid buildup or complications if the tube stops working properly during medical treatment.
Healthcare professionals and patients using Bard's NG sump tubes with ENFit connectors. Those with specific serial numbers listed in the recall are most at risk.
Check for the model EN0042180 with serial numbers NGDT1997, NGES3427, NGES4095, NGFV0834, NGFV3461, NGFW1886, NGFX5524, NGFY2527, NGGT3565. These tubes were sold with the UDI/DI 00801741113819.
Look for the serial numbers listed: NGDT1997, NGES3427, NGES4095, NGFV0834, NGFV3461, NGFW1886, NGFX5524, NGFY2527, NGGT3565.
Bard has received user complaints that these tubes sometimes don't drain stomach contents properly, which could lead to fluid buildup.
Check for the serial numbers NGDT1997, NGES3427, NGES4095, NGFV0834, NGFV3461, NGFW1886, NGFX5524, NGFY2527, or NGGT3565.
The recall does not specify a remedy, so contact Bard directly for guidance.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-0794-2024 — Bard Bard Hello, I own a Bard that is covered by recall Z-0794-2024 from Bard. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.