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FDAFDA · Food and drugs·Recall number Z-0341-2015

Arthroscopy Pack, catalog #900-2473 Used by medical staff to perform patient care procedures such as wound healing, suture removals, irrigate wounds, etc.

Published December 10, 2014 · Recall initiated: October 8, 2014

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Significant compromised sterility, not limited to potentially damaged packaging. Serious deficiencies in the manufacturing processes and uncontrolled and inadequate storage conditions increase the risk of contamination and may result in patient infection.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Customed, Inc
Distributor
US Distribution to Florida, New York and Puerto Rico..
Lot
Lot numbers 140513400
Risk classification
Class I
Area (FDA)
device
Country
United States

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