# FDA recall Z-1978-2023

> **Wilson-Cook Medical Inc.** · Class II · device recall initiated 2023-05-22.

## Product

Hemospray Endoscopic Hemostat:  Reference Part Numbers:  a) HEMO-7, REF G56572; b) HEMO-7-EU, REF G24663;

## Reason for recall

There are potential risks of the Hemospray powder adhering to the distal end of the endoscope, which can result in adhesion of the endoscope to tissue and consequent difficulty or inability to maneuver/remove the endoscope.

## Distribution

US Nationwide - Worldwide Distribution

## Key facts

- **Recall number:** Z-1978-2023
- **Recalling firm:** Wilson-Cook Medical Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-05-22
- **Report date:** 2023-06-28

- **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-1978-2023

## Citation

> AI Analytics. FDA recall Z-1978-2023. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-1978-2023. Source: US FDA. Licensed CC0.

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