# FDA recall Z-2170-2025

> **Stryker Corporation** · Class II · device recall initiated 2025-06-18.

## Product

Stryker, StrykeFlow , REF: 0250070500, 2, Disposable Suction/Irrigator without Disposable Tip

## Reason for recall

Due to complaints their is the potential that irrigation solution  may leaked into the handpiece and battery pack causing it to malfunction.

## Distribution

Worldwide - US Nationwide distribution including in the states of Alabama, Alaska, Arizona, 	Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, 	Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kansas, Kentucky, Louisiana, Maine, 	Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Montana, Nebraska, 	Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, 	Ohio, Oklahoma, Oregon, Pennsylvania, Puerto Rico, Rhode Island, South Carolina, South Dakota, Tennessee, Texas, Utah, Vermont, Virginia, Washington, West Virginia, Wisconsin, Wyoming and the countries of Argentina, Philippines, Singapore, China, Japan, Canada, Korea.

## Key facts

- **Recall number:** Z-2170-2025
- **Recalling firm:** Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-06-18
- **Report date:** 2025-07-30

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2170-2025

## Citation

> AI Analytics. FDA recall Z-2170-2025. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2170-2025. Source: US FDA. Licensed CC0.

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