# FDA recall Z-1174-2025

> **DeRoyal Industries Inc** · Class II · device recall initiated 2025-01-15.

## Product

DeRoyal AMG Suction Connector Tubing REF:  71-2083,  71-C506,  71-C510,  71-C512,  71-C520,    Tubing is intended for fluid movement

## Reason for recall

The tubing may not ensure that the yankauer stays intact, and secure to the tubing / yankauer connection for a tight seal. This could result in inadequate suction and cause delay in patient care.

## Distribution

U.S.:  ND, NY, VA, WV, NJ, TN, OK, TN, GA, OH, MN, AZ, WI, IL, MA, MD, MO, AR, MS, NY, MS, SC, HI, AR, UT, HI,  O.U.S.: Kuwait

## Key facts

- **Recall number:** Z-1174-2025
- **Recalling firm:** DeRoyal Industries Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-01-15
- **Report date:** 2025-02-26

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Powell, TN, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1174-2025

## Citation

> AI Analytics. FDA recall Z-1174-2025. Retrieved 2026-07-06 from https://api.ai-analytics.org/recall/Z-1174-2025. Source: US FDA. Licensed CC0.

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