FDAJanuary 13, 2021device

Covidien Parietex hydrophilic anatomical mesh 15 cm x 10 cm polyester left - Product Usage: designed for the repair of inguinal hernias via laparoscopic or posterior open procedures Item Code: TECT1510AL

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

The hazard

incorrect device is contained in the package. The packaging label indicates that the device is for left side use, the product inside the package is for right side use. Use of an opposite side mesh can result in implant failure and hernia recurrence

What to do

FDA enforcement status: Terminated

Brands named

covidien

Recall history

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

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