FDA recall record

Inspire Model 3028, IV Implantable Pulse Generator recall — FDA Z-2159-2024

There is a potential manufacturing defect which can lead to electrical leakage in the sensing circuit which causes a system malfunction and requires a…

Class Iclassification
Z-2159-2024official record ID
Jul 3, 2024report date

Recall record at a glance

Official recordZ-2159-2024
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmInspire Medical Systems Inc.
Report dateJul 3, 2024
Recall initiation dateMay 16, 2024
Quantity24 devices
LocationGolden Valley, MN, United States

Official product description

Inspire Model 3028, IV Implantable Pulse Generator

Why the product was recalled

There is a potential manufacturing defect which can lead to electrical leakage in the sensing circuit which causes a system malfunction and requires a revision surgery to replace the IPG,

Distribution information

Worldwide distribution - US Nationwide and the country of Germany.

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.

FDA source limitation: openFDA enforcement reports are a reference dataset, not a live public-alert or recall-lifecycle service. FDA notes that enforcement-report status may not be updated after classification. Confirm current actions with the FDA, recalling firm or appropriate healthcare professional when relevant.

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