FDAMay 29, 2020device

RUSCH LASERTUBE (Rubber), RES 102004, Sizes: a) I.D. mm 4,0, Product Code 102004-000040 b) I.D. mm 5,0, Product Code 102004-000050 c) I.D. mm 6,0, Product Code 102004-000060 d) I.D. mm 7,0, Product Code 102004-000070 e) I.D. mm 8,0, Product Code 102004-000080 Product Usage: Tracheal intubation du...

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

The hazard

Teleflex is initiating a voluntary recall for the above-mentioned products due to reports indicating that the laser guard foil partially separated and/or slightly detached at the edges in the presence of moisture.

What to do

FDA enforcement status: Terminated

Brands named

teleflex medicalteleflex

UPCs

102004000040102004000050102004000060102004000070102004000080

Recall history

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

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