FDA recall record

Maquet Datascope Corp - Cardiac Assist Division Cardiosave Rescue IABP, Part Number recall — FDA Z-0100-2019

There is a potential for interruption and/or inability to start therapy to the patient prior to or during use of Cardiosave IABP for users who are at…

Class Iclassification
Z-0100-2019official record ID
Nov 7, 2018report date

Recall record at a glance

Official recordZ-0100-2019
CategoryMedical Device Recalls
ClassificationClass I
FDA record statusOngoing
Recalling firmMaquet Datascope Corp - Cardiac Assist Division
Report dateNov 7, 2018
Recall initiation dateSep 20, 2018
QuantityN/A
LocationMahwah, NJ, United States

Official product description

Cardiosave Rescue IABP, Part Number 0998-UC-0800-83

Why the product was recalled

There is a potential for interruption and/or inability to start therapy to the patient prior to or during use of Cardiosave IABP for users who are at altitudes above 3200 Ft.

Distribution information

US Nationwide; Internationally to 77 countries

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: Press Release.

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.

Related recall records

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