# FDA recall Z-2051-2021

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2021-06-15.

## Product

EASYGRIP FLO-41 US.  For delivering hemostatic agents to bleeding sites through a trocar.

## Reason for recall

There is a discrepancy in the expiry date encoded into the 2D barcode. The correct expiration date is the human-readable date

## Distribution

United States, Australia, Hong Kong, New Zealand, Belgium, Cyprus, Ireland, Italy, Netherlands, Norway, Portugal, Spain, Sweden, and United Kingdom.

## Key facts

- **Recall number:** Z-2051-2021
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-06-15
- **Report date:** 2021-07-21
- **Termination date:** 2024-01-12

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Deerfield, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2051-2021

## Citation

> AI Analytics. FDA recall Z-2051-2021. Retrieved 2026-09-08 from https://api.ai-analytics.org/recall/Z-2051-2021. Source: US FDA. Licensed CC0.

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