FDAFebruary 5, 2015device

Zip 8i Surgical Skin Closure Device; for incisions up to 8 cm. Product number PS2080 Indicated for use during and after skin incision procedures to approximate skin and hold together skin edges until healing can take place.

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

The hazard

The manufacturers seal may not be present on the Nylon pouch resulting in lack of assurance for sterility.

What to do

FDA enforcement status: Terminated

Brands named

zipline medicalzipline

Recall history

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

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