FDAMay 30, 2019device

Anti-fog solution packaged in a Tyvek peel pouch and it is placed into various kits. Kit are labeled as follows: ROBOTIC GENERAL, LAP CHOLE, GENERAL LAPAROSCOPY PACK-LF, T&A PACK, LAP CHOLE PACK-LF, LAPAROSCOPY PACK-LF, EAR ACCESSORY PACK, RF LAP CHOLEPACK (LCLUI)642-LF, GEN LAPAROSCOPY PACK-LF, ...

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

The hazard

The Anti-Fog Solution may not defog properly due to a degradation in the chemical properties.

What to do

FDA enforcement status: Ongoing

Brands named

medline

Recall history

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

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