Teleflex Medical recalls RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0

Recall date

April 1, 2019

Source

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

Recall number

Z-1682-2019

FDA classification

Class II

Brand / firm

Teleflex Medical

Sold / distributed

Nationwide

Why it was recalled

The firm received reports indicating that the laser guard foil partially separated and/or slightly detached at the edges.

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

What was recalled

RUSCH LASERTUBE (Rubber), Order No. : 102004-000040, REF 102004, SIZE I.D. mm 4,0