CLASS II ONGOING Device recall · Reported 31 Jan 2024 · FDA Enforcement Report
Bard¿ Nasogastric Sump Tube with ENFit recalled by C.R. Bard
C.R. Bard is recalling Bard¿ Nasogastric Sump Tube with ENFit. The recall was initiated on 20 Dec 2023 and the FDA has classified it as Class II.
Check your package
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-0791-2024
- 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 ENFit, 12Fr., 48in Long, REF EN0042120
Where it was distributed
US
Questions about this recall
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 00801741113789, Lot/Serial Numbers: NGDU4227, NGDX0616, NGEQ3058, NGER3569, NGFN0711, NGFS4430, NGFT1895, NGFT5466, NGFU2448, NGFV1675, NGFW1843, NGFX0166, NGFY2526, NGGR2645, NGGT2116, NGHQ2394
Where was it sold?
US
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 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
Other products in this recall event
16 other products · FDA event 93679This product is part of a recall event; the main page for the event is Bard¿ Nasogastric Sump Tube with ENFit recalled by C.R. Bard.
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