Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0799-2024 — Bard¿ Nasogastric Sump Tube with PreVent¿ Anti-Reflux Filter with ENFit, 16Fr., 48in Long, REF EN0046160

U.S. FDA — Device Enforcement · United States · 2023-12-20 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0799-2024
Date of alert
2023-12-20
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
C.R. Bard Inc
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
00801741113253
Reported risk: 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.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.