Medical device recalls Moderate risk

Kentec Medical, Inc recalls Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes. Sterile and single use only. Catalog number EN…

Recall date
January 17, 2020
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2517-2020
FDA classification
Class II
Brand / firm
Kentec Medical, Inc
Sold / distributed
US: CA, IA, and VA

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

Ameritus Medical Products ENFit Polyurethane and Silicone Feeding Tubes. Sterile and single use only. Catalog number ENF-80P-50 (8 fr. 50 cm ENFit Enteral Feeding Tube).

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