# FDA recall Z-1544-2021

> **Infusion Pump Repair** · Class I · device recall initiated 2021-03-26.

## Product

Alaris Pump Module, Model 8100, serviced/repaired by Infusion Pump Repair with an impacted bezel repair part

## Reason for recall

Bezel repair parts used, not by the original manufacturer, to service and repair infusion pump modules, may over time experience cracking or separation of the posts from the bezel. The separation of one or more bezel repair part posts may result in free flow, over infusion, under infusion or interruption of infusion.

## Distribution

California

## Key facts

- **Recall number:** Z-1544-2021
- **Recalling firm:** Infusion Pump Repair
- **Classification:** Class I
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2021-03-26
- **Report date:** 2021-05-19

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Irvine, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1544-2021

## Citation

> AI Analytics. FDA recall Z-1544-2021. Retrieved 2026-06-10 from https://api.ai-analytics.org/recall/Z-1544-2021. Source: US FDA. Licensed CC0.

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