US Drug Recall Register
Class I · High risk Terminated Initiated Feb 4, 2022 (5 years ago)

PARAGARD T380A (intrauterine copper contraceptive), 1 unit per carton together with an…

Class I — High risk. Reasonable probability of serious harm or death.

Why it was recalled

Non-sterility

What was recalled

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

Recalling firm
CooperSurgical, Inc
NDC code
51285-204-01
Origin
NY, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0643-2022

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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