FDA recall record

LivaNova SMART PERFUSION PACK INSPIRE 8S - Product Usage: The affected product is a recall — FDA Z-1389-2020

Perfusion tubing pack was packaged with the incorrect cuvette.

Class IIIclassification
Z-1389-2020official record ID
Mar 4, 2020report date

Recall record at a glance

Official recordZ-1389-2020
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusTerminated
Recalling firmLivaNova USA Inc.
Report dateMar 4, 2020
Recall initiation dateJul 3, 2019
Quantity27 packs
LocationArvada, CO, United States

Official product description

LivaNova SMART PERFUSION PACK INSPIRE 8S - Product Usage: The affected product is a perfusion tubing pack use in surgical procedures requiring extracorporeal support. The perfusion tubing packs include the cuvette used with equipment to monitor blood.

Why the product was recalled

Perfusion tubing pack was packaged with the incorrect cuvette.

Distribution information

US Nationwide distribution in the state of IL.

How to read the classification

FDA Class III generally covers situations in which use of or exposure to the product is not likely to cause adverse health consequences. The classification displayed here is taken from the FDA enforcement record.

Additional record details

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

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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