# FDA recall Z-0768-2021

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2020-11-10.

## Product

MiniCap Extended Life PD Transfer Set

## Reason for recall

Potential for no-flow and leaks under the twist clamp.

## Distribution

Worldwide and US (Nationwide), Canada, Brazil, Mexico, Bermuda, and Indonesia

## Key facts

- **Recall number:** Z-0768-2021
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-11-10
- **Report date:** 2021-01-13
- **Termination date:** 2023-03-24

- **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-0768-2021

## Citation

> AI Analytics. FDA recall Z-0768-2021. Retrieved 2026-07-02 from https://api.ai-analytics.org/recall/Z-0768-2021. Source: US FDA. Licensed CC0.

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