# FDA recall Z-2432-2023

> **Datascope Corp.** · Class I · device recall initiated 2023-07-31.

## Product

Cardiosave Rescue Intra-Aortic Balloon Pumps (IABP), Part Numbers 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85

## Reason for recall

Users were reporting that the device was not charging as expected. It was discovered that users were unaware that the Cardiosave console was not completely inserted into the hospital cart. If the console is not fully inserted back into the cart the battery(ies) will not charge.

## Distribution

Worldwide - US Nationwide distribution.

## Key facts

- **Recall number:** Z-2432-2023
- **Recalling firm:** Datascope Corp.
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-07-31
- **Report date:** 2023-09-06

- **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-2432-2023

## Citation

> AI Analytics. FDA recall Z-2432-2023. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-2432-2023. Source: US FDA. Licensed CC0.

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