FDA recall record

Datascope Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Model Number 0998-00-0800-55 recall — FDA Z-1907-2023

The digital IFUs provided with the Cardiosave IABP during the software update to version D.00 incorrectly annotated compliance to standard 60601-1-12:2014…

Class IIIclassification
Z-1907-2023official record ID
Jun 21, 2023report date

Recall record at a glance

Official recordZ-1907-2023
CategoryMedical Device Recalls
ClassificationClass III
FDA record statusOngoing
Recalling firmDatascope Corp.
Report dateJun 21, 2023
Recall initiation dateMay 4, 2023
Quantity4 units
LocationMahwah, NJ, United States

Official product description

Cardiosave Hybrid Intra-Aortic Balloon Pumps (IABP), Model Number 0998-00-0800-55, Part Number 0998-00-0800-XX

Why the product was recalled

The digital IFUs provided with the Cardiosave IABP during the software update to version D.00 incorrectly annotated compliance to standard 60601-1-12:2014 within the updated IFU.

Distribution information

International distribution in the country of Germany.

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: 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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Class IIIFDA: OngoingDatascope Corp.