Unomedical As recalls Contact Detach, 8mm, 23", G29; Contact Detach 8 mm, 43", G29; Contact Detach, 6mm, 23" G29; Infusion Set, Contact Detac…

Recall date

November 7, 2014

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-0356-2017

FDA classification

Class II

Brand / firm

Unomedical As

Sold / distributed

Worldwide Distribution - US including CA, IN, PA, and Internationally to Canada, Korea, and Japan.

Why it was recalled

Tubing detachment

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

What was recalled

Contact Detach, 8mm, 23", G29; Contact Detach 8 mm, 43", G29; Contact Detach, 6mm, 23" G29; Infusion Set, Contact Detach, 6mm x 23"; Infusion Set, Contact Detach, 6mm x 32"; Infusion Set, Contact Detach, 8mm x 23"; Infusion Set, Contact Detach, 8mm x 32" The products are used in combination with insulin infusion pumps for continuous subcutaneous infusion of insulin