FDAMarch 10, 2015device

(S) TUBE SET 1/4" X 10' (0.64 cm X 304.8 cm) with 7/8" (2.22 cm) Adaptor, Sterile, REF 24155, QTY 10/CS, STERILE EO, NO LATEX Intended use: The smoke evacuator and accessories are intended to evacuate the smoke created by electrosurgery, laser surgery, or power tool surgical procedures. Locations...

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

The hazard

This recall is being conducted because a cohesive band used to package the devices contains latex and the product is not labeled as required by 21 CFR 801.437; it does not contain Caution: The Packaging of This Product Contains Natural Rubber Latex Which May Cause Allergic Reactions.

What to do

FDA enforcement status: Terminated

Brands named

microtek medicalmicrotek

Recall history

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

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