FDAFebruary 4, 2022drug

PARAGARD T380A (intrauterine copper contraceptive), 1 unit per carton together with an insertion tube and solid white rod in a Tyvek polyethylene pouch, Rx Only, Manufactured by Teva Women's Health Inc. a subsidiary of Teva Pharmaceuticals USA, Inc., North Wales, PA 19454, NDC 51285-204-01

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

The hazard

Non-sterility

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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