FDAMarch 13, 2015device

Integra¿ Flowable Wound Matrix Size 3cc 1 unit/box single use, sterile device Rx Only Model Number FWD301 (US) & FDR301 (Non-US) Flowable Wound Matrix is comprised of the following components which are provided in a sealed and sterilized Tyvek / plastic tray: - An empty plastic syringe with Luer-...

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

The hazard

A lot of Flowable Wound Matrix that has been distributed to customers in late 2013 / early 2014 was verified as not meeting stability acceptance criteria for the attributes of visual appearance during dispensing and force vs. displacement (force needed for product to be extruded from the syringe).

What to do

FDA enforcement status: Terminated

Brands named

integra lifesciencesintegra

UPCs

30500029325030500029325130500029861610500028786105000288118

Recall history

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

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