FDAMarch 10, 2015device

FREEDOMAIRE(R) MOTOR MODULE, REF 11112STK, QTY 1/CS, NON STERILE, NO LATEX The Surgical Helmet System is intended to be worn by surgical personnel to provide barrier between the operating environment and the surgical personnel in order to protect against contamination, body fluids and microorgani...

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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