# FDA recall Z-0572-2022

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2022-01-07.

## Product

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Short, 5C4483

## Reason for recall

Cleaning products, containing, but not limited to, hydrogen peroxide, bleach, alcohol, or antiseptic agents and solvent, such as those containing acetone, toluene, xylene, or cyclohexanone may cause damage, such as leaking or cracking, to the MiniCap Extended Life PD transfer sets.

## Distribution

Worldwide

## Key facts

- **Recall number:** Z-0572-2022
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-01-07
- **Report date:** 2022-02-16

- **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-0572-2022

## Citation

> AI Analytics. FDA recall Z-0572-2022. Retrieved 2026-06-14 from https://api.ai-analytics.org/recall/Z-0572-2022. Source: US FDA. Licensed CC0.

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