Teleflex Medical recalls Pilling Modular Verres Body/Obturator, Product Code 140880

Recall date

January 8, 2015

Source

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

Recall number

Z-1178-2016

FDA classification

Class II

Brand / firm

Teleflex Medical

Sold / distributed

US Distribution to the state of : UT

Why it was recalled

Packaging error in which customers who ordered product code 140880 (Verres cannula for use with a separately available needle tip) were incorrectly provided with product code 140878 (Verres cannula with integral needle tip).

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

What was recalled

Pilling Modular Verres Body/Obturator, Product Code 140880