Bard recalls PreVent Anti-Reflux Filters with ENFit connectors due to reported inadequate suction, decompression, and drainage during use. Affected units have specific serial numbers and were sold in the U.S. from 2020 to 2023.
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 PreVent Anti-Reflux Filters with ENFit connectors because users reported reduced suction, decompression, and drainage. This could lead to improper drainage of fluids during medical procedures, potentially causing complications.
The filters may not provide adequate suction, leading to reduced drainage of fluids during medical procedures. This could cause complications such as fluid buildup or improper treatment outcomes.
Patients using Bard PreVent Anti-Reflux Filters with ENFit connectors for medical procedures are most at risk. The recall affects specific serial numbers sold between 2020 and 2023.
Check for serial numbers listed: NGEV2409, NGEY1492, NGEY2717, NGEZ0908, NGEZ1657, NGEZ2692, NGFQ4105, NGFR1077, NGFR2312, NGFR3259, NGFS1627, NGFS4431, NGFT5468, NGFU1877, NGFU3837, NGFV1652, NGFV3513, NGFW1856, NGFX0167, NGFX2672, NGFX5611, NGGP3169, NGGT3611. These units were sold in the U.S. from 2020 to 2023.
Look for the specific serial numbers listed in the recall notice to determine if your filter is affected.
Bard has received user complaints reporting that during use of these filters, inadequate or reduced suction, decompression, and drainage occurred.
The recall does not specify a remedy, so contact Bard directly for guidance on next steps.
The recall indicates potential issues with suction and drainage, which could lead to complications during medical procedures.
We’ve drafted a message you can send Bard to request your refund or repair — edit it as you like.
Subject: Recall Z-0795-2024 — Bard Bard Hello, I own a Bard that is covered by recall Z-0795-2024 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.
