CooperSurgical, Inc recalls PARAGARD T380A (intrauterine copper contraceptive), 1 unit p
See all recalls from CooperSurgical, Inc →Recalled 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
Hazard / Issue
Non-sterility
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot # 517001,Exp 1/2024
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for PARAGARD T380A (intrauterine copper →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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