# FDA recall Z-0819-2025

> **Applied Medical Technology Inc** · Class II · device recall initiated 2024-11-26.

## Product

AMT Mini Enteral Extension Set, 12" Right Angle Feeding Set with Y-Port. Model/Catalog Number: E6-1222

## Reason for recall

The extension sets subject to this recall have ENFit connections, although they should have non- ENFit connections. ENFit connectors will only fit with other ENFit-compatible devices, and will not fit with non-ENFit connectors.

## Distribution

US Distribution to states of: CA, CT, FL, GA, IL, MA, MD, MO, NC, NJ, NY, OH, OK, PA, SC, TX, VA, WA

## Key facts

- **Recall number:** Z-0819-2025
- **Recalling firm:** Applied Medical Technology Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2024-11-26
- **Report date:** 2025-01-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Brecksville, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0819-2025

## Citation

> AI Analytics. FDA recall Z-0819-2025. Retrieved 2026-06-26 from https://api.ai-analytics.org/recall/Z-0819-2025. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
