FDAApril 1, 2019device

RUSCH LASERTUBE (Rubber), Order No. : 102004-000070, REF 102004, SIZE I.D. mm 7,0

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Terminated

Brands named

teleflex medicalteleflex

UPCs

102004000070

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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