# FDA recall Z-0831-2022

> **Baxter Healthcare Corporation** · Class II · device recall initiated 2022-02-25.

## Product

MiniCap Extended Life PD Transfer Set Product Codes: 5C4482S, R5C4482, R5C4483, R5C4484

## Reason for recall

Devices distributed lacked regulatory clearance.

## Distribution

US Nationwide distribution in the states of California, Colorado, District of Columbia, Delaware, Florida, Georgia, Illinois, Louisiana, Michigan, Missouri, New Mexico, New York, Ohio, Oklahoma, Pennsylvania, and Texas.

## Key facts

- **Recall number:** Z-0831-2022
- **Recalling firm:** Baxter Healthcare Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2022-02-25
- **Report date:** 2022-04-06

- **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-0831-2022

## Citation

> AI Analytics. FDA recall Z-0831-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0831-2022. Source: US FDA. Licensed CC0.

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