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U.S. Department of Health and Human Services

Medsun Reports

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Type of Device:
Device intrauterine
Device Brand Name:
Device Manufacturer's Name:
Date of this Report:
Describe the Event
or Problem:
Patient had Paragard IUD in situ for 8.5 years. Presented to clinic for IUD removal. Upon removal of device, noted the copper coil was missing from the long portion of IUD. Copper was present on "T" arms of device and both arms were intact.
Manufacturer response for ParaGard IUD T380a, (brand not provided) (per site reporter)
Leadership working with rep to resolve issue.
the device(s) may have
caused or contributed to:
Potential for patient harm
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