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

Recall Z-1357-2018 — Bard(R) Premature Infant Feeding tube, ENFit(TM), REF EN0036430 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term tube feeding, lavage fl

U.S. FDA — Device Enforcement · United States · 2018-02-27 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1357-2018
Date of alert: 2018-02-27
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: C.R. Bard, Inc.
Product category: device
Product type: Devices

Reported risk: BMD has identified that the product code/lot number combination identified above may have ineffectively fused tubing and ENFit(TM) connector.

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.

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.

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