FDAFDA · Food and drugs·Recall number D-0643-2022
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
Published February 23, 2022 · Recall initiated: February 4, 2022
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Non-sterility
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- CooperSurgical, Inc
- Distributor
- US Nationwide
- Lot
- Lot # 517001,Exp 1/2024
- Risk classification
- Class I
- Area (FDA)
- drug
- Country
- United States
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