# FDA recall Z-2263-2024

> **Zyno Medical LLC** · Class II · device recall initiated 2024-06-04.

## Product

Zyno Medical Z800, Z800F, Z800W, and Z800WF Infusion Pumps

## Reason for recall

Zyno Medical has found that certain Z800, Z800F, Z800W, and Z800WF pumps have faulty power supply modules that will not provide a charge to the rechargeable battery within the pump. This may lead to the battery having insufficient or no charge available to the pump when it is unplugged from the AC mains power.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2263-2024
- **Recalling firm:** Zyno Medical LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-06-04
- **Report date:** 2024-07-10

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Natick, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2263-2024

## Citation

> AI Analytics. FDA recall Z-2263-2024. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-2263-2024. Source: US FDA. Licensed CC0.

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