Bard recalls NG Sump Tubes with PreVent Anti-Reflux Filter due to reported inadequate suction and drainage. Affected models include ENFit 10Fr 36in tubes with specific serial numbers.
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 tubes that may cause inadequate suction or drainage during use. This could lead to complications like fluid buildup or infection if not properly managed.
The tubes may not drain stomach contents effectively, leading to reduced suction and potential fluid buildup. This could cause complications like aspiration or infection if the tube is not functioning properly.
Healthcare professionals using Bard NG Sump Tubes with ENFit connectors are most at risk, particularly those with specific serial numbers listed in the recall.
Check for the model: Bard Nasogastric Sump Tube with PreVent Anti-Reflux Filter, ENFit 10Fr, 36in long. Look for serial numbers like NGDX0768, NGDZ3314, or others listed in the recall.
Compare your tube's serial number with the list of affected numbers provided in the recall notice.
If you have the affected tube, consult your healthcare provider about alternative tube options or proper use.
Bard has received user complaints that the tubes may not drain stomach contents effectively, leading to inadequate suction and drainage.
The affected models include Bard Nasogastric Sump Tubes with PreVent Anti-Reflux Filter, ENFit 10Fr, 36in long, with serial numbers like NGDX0768, NGDZ3314, NGER3568, and others listed in the recall.
No, but you should check your tube's serial number and contact your healthcare provider if you have an affected model.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-0796-2024 — Bard Bard Hello, I own a Bard that is covered by recall Z-0796-2024 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.
