FDA recall record

CooperSurgical PARAGARD T380A recall — FDA D-0643-2022

Non-sterility

Class Iclassification
D-0643-2022official record ID
Feb 23, 2022report date

Recall record at a glance

Official recordD-0643-2022
CategoryDrug Recalls
ClassificationClass I
FDA record statusTerminated
Recalling firmCooperSurgical, Inc.
Report dateFeb 23, 2022
Recall initiation dateFeb 4, 2022
Quantity48,645 cartons
LocationNorth Tonawanda, NY, United States

Official product description

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

Why the product was recalled

Non-sterility

Distribution information

US Nationwide

How to read the classification

FDA Class I indicates a situation in which there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. The classification shown here comes directly from the FDA enforcement record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Letter.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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Related recall records

Other records from the same recalling company are shown first when available.

Medical DeviceJul 30, 2025

CooperSurgical HSG Procedure Tray recall — FDA Z-2135-2025

The HSG Procedure Trays and Endosee System Convenience Kits contain non-sterile iodine pouches, however the peel away lid labels incorrectly identify the iodine pouches as sterile.

Class IIFDA: OngoingCooperSurgical, Inc.