Medical device recalls Moderate risk

Medical Components, Inc dba MedComp recalls Duo-Flow XTP Straight Full Set; Hemodialysis catheter insertion kits, AAC02106 AAC02107 AAC02108

Recall date
July 12, 2018
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2932-2018
FDA classification
Class II
Brand / firm
Medical Components, Inc dba MedComp
Sold / distributed
Nationwide distribution; worldwide distribution.

Why it was recalled

The suture wings have the potential to crack or break. Potential patient injury includes catheter dislocation, bleeding, and air emboli. The firm has received six complaints (29 broken suture wings) to date for malfunction, without serious injury or death.

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

What was recalled

Duo-Flow XTP Straight Full Set; Hemodialysis catheter insertion kits, AAC02106 AAC02107 AAC02108

Get recall alerts

Free email alert whenever Medical Components, Inc dba MedComp has a new recall — straight from official government data. Unsubscribe anytime.

More recalls from: Medical Components, Inc dba MedComp