Bard recalls NG Sump Tubes with ENFit connectors due to reported inadequate suction and drainage. Affected models include specific serial numbers and sizes. Consumers should 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 nasogastric sump tubes with ENFit connectors because users report reduced suction and drainage. This could lead to improper stomach emptying and potential complications if the tube isn't working correctly.
The tubes may not create enough suction or drainage, leading to stomach contents not being properly emptied. This could cause discomfort, infection, or other complications if the tube fails to function as intended.
Healthcare professionals and patients using Bard's NG Sump Tubes with ENFit connectors are affected. Those with the specific model numbers listed are most at risk.
Check for the model name 'Bard Nasogastric Sump Tube with ENFit, 14Fr., 48in Long' and serial numbers like NGEP0376 or NGEQ3035. The product was sold with specific reference numbers.
Reach out to Bard directly for specific instructions on how to handle the recalled tubes.
Bard has received user complaints reporting inadequate or reduced suction, decompression, and drainage with these tubes.
The affected models include serial numbers such as NGEP0376, NGEQ3035, NGES3428, and others listed in the recall notice.
The recall does not require immediate stop use; however, users should contact Bard for guidance on handling the affected tubes.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-0792-2024 — Bard Bard Hello, I own a Bard that is covered by recall Z-0792-2024 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.
