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

Recall Z-2518-2020 — Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes. Sterile and single use only. Catalog number ENF-Y60P-50 (6 fr. 50 cm ENFit Enteral Feeding Tube with Y-Port).

U.S. FDA — Device Enforcement · United States · 2020-01-17 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2518-2020
Date of alert
2020-01-17
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Kentec Medical, Inc
Product category
device
Product type
Devices
Reported risk: Feeding tube plastic tethered closure cap may possibly fracture or break. Possible health hazards: (1) Enteral feeding and medication administration could be possibly delayed, until replacement tube is placed into patient (2) Patient could be unnecessarily overexposed to radiation if multiple x-rays are needed to confirm placement of a new tube, if x-ray is used as the placement confirmation method.
Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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