# FDA recall Z-0756-2021

> **Lidco Ltd** · Class II · device recall initiated 2020-11-19.

## Product

CM 50-001-01 Injectate Kit, accessory device to LiDCOunity v2 Monitor - Product Usage: intended to administer lithium dilution indicator (tube administrative set).

## Reason for recall

The expiration date on labeling is incorrect.

## Distribution

Worldwide distribution - US Nationwide distribution in the state of IL and the country of Kuwait.

## Key facts

- **Recall number:** Z-0756-2021
- **Recalling firm:** Lidco Ltd
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-11-19
- **Report date:** 2021-01-06
- **Termination date:** 2022-09-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** London, N/A, United Kingdom

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0756-2021

## Citation

> AI Analytics. FDA recall Z-0756-2021. Retrieved 2026-07-27 from https://api.ai-analytics.org/recall/Z-0756-2021. Source: US FDA. Licensed CC0.

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