# FDA recall Z-2057-2018

> **Stryker Corporation** · Class II · device recall initiated 2017-12-21.

## Product

3910-090-800 ASSY, PKG, 8.0MM X 90MM DRI-LOK THREADED CANNULA, 5 units per box.    The Disposable Cannula device is designed to be used as a port of entry for arthroscopic instruments into the joints.

## Reason for recall

Inadvertent shipment of expired units.

## Distribution

US distribution to Massachusetts only..

## Key facts

- **Recall number:** Z-2057-2018
- **Recalling firm:** Stryker Corporation
- **Classification:** Class II
- **Product type:** device
- **Status:** Completed
- **Initiation date:** 2017-12-21
- **Report date:** 2018-06-13

- **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-2057-2018

## Citation

> AI Analytics. FDA recall Z-2057-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-2057-2018. Source: US FDA. Licensed CC0.

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