# FDA recall Z-0266-2020

> **Datascope Corp.** · Class II · device recall initiated 2019-10-03.

## Product

Low Level Output Cable   Interface to Philips Monitor For Use With Cardiosave and CS300 Intra-Aortic Balloon  Pumps (IABPs), Part Number 0012-00-1589-03

## Reason for recall

One lot of "Low Level Output Cable - Interface to Philips Monitor" was received from the supplier with an incorrect cable in the packaging.

## Distribution

Distributed to CA, GA, and TX.

## Key facts

- **Recall number:** Z-0266-2020
- **Recalling firm:** Datascope Corp.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-10-03
- **Report date:** 2019-11-13
- **Termination date:** 2021-01-08

- **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-0266-2020

## Citation

> AI Analytics. FDA recall Z-0266-2020. Retrieved 2026-07-05 from https://api.ai-analytics.org/recall/Z-0266-2020. Source: US FDA. Licensed CC0.

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