CooperSurgical, Inc recalls PARAGARD T380A (intrauterine copper contraceptive), 1 unit per carton together with an insertion tube and solid white ro
Recalled February 23, 2022 · FDA recall D-0643-2022 · CooperSurgical
Hazard
Non-sterility · FDA Class I
Units
48,645 cartons
Sold at
US Nationwide
Description
Non-sterility
Product
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
Manufacturer(s)
CooperSurgical, Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →