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FDAAugust 19, 2019device

LEEP Return Patient Pads (10/ box) Model # 6050Pl used in electrosurgical procedures.

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

The hazard

Discrepancy between the correct expiration dates on the individual pouches inside the boxes and incorrect expiration dates on the outer boxes, where the month and day were reversed.

What to do

FDA enforcement status: Terminated

Brands named

coopersurgical

Recall history

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

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