FDAJuly 8, 2020device

M-Close Kit, REF 27-101; a disposable, ligature passing, suturing apparatus and needle guide for the abdominal wall

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

The hazard

The plastic housing on the device may fracture

What to do

FDA enforcement status: Terminated

Brands named

new wave endo surgical

UPCs

00850009417022

Recall history

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

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