# FDA recall Z-2541-2019

> **Wilson-Cook Medical Inc.** · Class II · device recall initiated 2019-07-24.

## Product

Hemospray Endoscopic Hemostat

## Reason for recall

Potential for Hemospray device to be unable to spray powder due to misassembly of devices.

## Distribution

Nationwide distribution to CA, CO, CT, FL, IL, IN, KY, LA, MN, MO, NC, NJ, NY, OH, PA, RI, SD, TX, VA, WA.      International distribution to Canada, Austria, Belgium, Cyprus, Denmark, France, Germany, Greece, Italy, Portugal, Spain, and United Kingdom.

## Key facts

- **Recall number:** Z-2541-2019
- **Recalling firm:** Wilson-Cook Medical Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-24
- **Report date:** 2019-09-25
- **Termination date:** 2020-06-15

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Winston Salem, NC, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2541-2019

## Citation

> AI Analytics. FDA recall Z-2541-2019. Retrieved 2026-07-05 from https://api.ai-analytics.org/recall/Z-2541-2019. Source: US FDA. Licensed CC0.

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