# FDA recall Z-3133-2017

> **Baxter Healthcare Corp** · Class II · device recall initiated 2017-09-01.

## Product

Baxter Amia Automated Peritoneal Dialysis Set with Cassette, REF 5C5479

## Reason for recall

The firm received increased customer complaints for Missing Red Line, Patient Slow Flow, Solution Slow Flow, and Inadequate Drain alerts on certain lots of the AMIA Automated Peritoneal Dialysis Set with Cassette.

## Distribution

nationwide, Canada

## Key facts

- **Recall number:** Z-3133-2017
- **Recalling firm:** Baxter Healthcare Corp
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-09-01
- **Report date:** 2017-09-20
- **Termination date:** 2019-08-27

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mountain Home, AR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-3133-2017

## Citation

> AI Analytics. FDA recall Z-3133-2017. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-3133-2017. Source: US FDA. Licensed CC0.

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