# FDA recall Z-2227-2018

> **The Seaberg Company Inc** · Class II · device recall initiated 2018-05-02.

## Product

Part #: SAM XT-C, Model: Hi-Viz Orange or Civilian

## Reason for recall

Based on internal testing, results indicated a possible failure of the stitches securing the buckle to the nylon belt could occur, posing a potential risk when used on a human patient to stop arterial blood flow. There is a remote chance that a serious injury and/or death could occur as a result of the failure of the device.

## Distribution

USA: CA, MD, OH, FL, ID, CO, CT, OR, AZ, IL, ME, MO, NY, SC, MI, AR, MT, CT, WA, TX, KY, NC, NJ, PA    OUS: Australia, Canada, China, Columbia, Costa Rica, Europe (EU), Hong Kong, Iceland, India, Iraq, Israel, Japan, Kenya, Korea, Lebanon, Malaysia, Russia, Saudi Arabia, Singapore, South Africa, Thailand, UAE

## Key facts

- **Recall number:** Z-2227-2018
- **Recalling firm:** The Seaberg Company Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2018-05-02
- **Report date:** 2018-06-20
- **Termination date:** 2020-07-01

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wilsonville, OR, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2227-2018

## Citation

> AI Analytics. FDA recall Z-2227-2018. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-2227-2018. Source: US FDA. Licensed CC0.

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