CLASS II ONGOING Device recall · Reported 31 Jan 2024 · FDA Enforcement Report

Bard¿ Nasogastric Sump Tube recalled by C.R. Bard

C.R. Bard is recalling Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit. The recall was initiated on 20 Dec 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUDI/DI 00801741113260, Lot/Serial Numbers: NGDT2000, NGDX0518, NGEW1822, NGEW3855, NGEX0043, NGEX1998, NGEZ2693, NGFP0406, NGFP3519, NGFR0244, NGFT0418, NGFT3481, NGFU3821, NGFV0785, NGFV1654, NGFV3445, NGFW1906, NGFX0169, NGFX2674, NGFX5527, NGGP3171

Quantity recalled57159 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number: Z-0800-2024
FDA event ID: 93679
Recalling firm: C.R. Bard, Covington, GA
Classification: Class II
Status: Ongoing
Recall initiated: 20 Dec 2023
FDA classified: 25 Jan 2024
Reported: 31 Jan 2024
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

20 Dec 2023	Recall initiated by company
25 Jan 2024	Classified by FDA	+36 days
31 Jan 2024	Published in enforcement report	+6 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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.

Product as listed by the FDA

Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 18Fr., 48in Long, REF EN0046180

Where it was distributed

Stores named: Walmart

Questions about this recall

Is Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit recalled?

Yes. C.R. Bard recalled Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit on 20 Dec 2023. The recall is Class II and its status is Ongoing. Recall number Z-0800-2024.

Why was it recalled?

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.

Which lots are affected?

UDI/DI 00801741113260, Lot/Serial Numbers: NGDT2000, NGDX0518, NGEW1822, NGEW3855, NGEX0043, NGEX1998, NGEZ2693, NGFP0406, NGFP3519, NGFR0244, NGFT0418, NGFT3481, NGFU3821, NGFV0785, NGFV1654, NGFV3445, NGFW1906, NGFX0169, NGFX2674, NGFX5527, NGGP3171

Where was it sold?

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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