Bard recalls NG Sump Tubes with ENFit connectors due to reported inadequate suction and drainage. Affected units have specific model numbers and serial ranges. 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 certain nasogastric tubes that may not drain properly, leading to reduced suction and potential complications. This affects medical users who rely on these tubes for feeding or drainage.
The tubes may not drain properly during use, causing inadequate suction and decompression. This could lead to complications like fluid buildup or infection if the tube is not functioning correctly.
Medical professionals and patients using Bard's NG Sump Tubes with ENFit connectors are affected. Those with the specific model numbers and serial ranges listed are most at risk.
Check for model numbers starting with NGD and serial numbers like NGDU4286, NGDX0519, or similar in the list provided. These tubes have ENFit connectors and are 18Fr, 48 inches long.
Identify the model number and serial number on the tube to confirm if it is affected.
Reach out to Bard directly for assistance with the recall and possible remedies.
Bard has received user complaints about inadequate suction and drainage with these tubes.
Affected units include model numbers starting with NGD and serial numbers like NGDU4286, NGDX0519, NGES3430, and others listed in the recall notice.
No, but you should check if your tube is affected and contact Bard 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-0805-2024 — Bard Bard Hello, I own a Bard that is covered by recall Z-0805-2024 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.
