# FDA recall Z-1462-2023

> **Datascope Corp.** · Class II · device recall initiated 2023-04-04.

## Product

MAQUET CARDIOSAVE hybrid Intra-Aortic Balloon Pump, Model Number 0998-XX-0800-32

## Reason for recall

The power cord supplied (Type J plug end) for the Cardiosave Hybrid IABP to Brazil is incompatible with the Brazilian Type N power receptacle.

## Distribution

International distribution in the country of Brazil.

## Key facts

- **Recall number:** Z-1462-2023
- **Recalling firm:** Datascope Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-04-04
- **Report date:** 2023-05-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mahwah, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1462-2023

## Citation

> AI Analytics. FDA recall Z-1462-2023. Retrieved 2026-08-01 from https://api.ai-analytics.org/recall/Z-1462-2023. Source: US FDA. Licensed CC0.

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