# FDA recall Z-1281-2022

> **Beaver Visitec International, Inc.** · Class II · device recall initiated 2022-04-26.

## Product

BVI Wet -Field Eraser, 18GA Blunt Tip, 45Deg.-Intended to remove tissue and control bleeding by the use of high frequency electrical current   Part Number: 221251

## Reason for recall

Boxes labeled as Wet-Field Eraser, 18GA Blunt Tip, 45Deg., were shipped containing incorrect product a Wet-Field Eraser, 18GA Bevel Tip, Straight, Part Number: 221250

## Distribution

US Nationwide distribution in the states of AZ, CA, CT, DC, FL, GA, IN, MA, MN, NV, SC, TX, WA.

## Key facts

- **Recall number:** Z-1281-2022
- **Recalling firm:** Beaver Visitec International, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-04-26
- **Report date:** 2022-06-29

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Waltham, MA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1281-2022

## Citation

> AI Analytics. FDA recall Z-1281-2022. Retrieved 2026-08-11 from https://api.ai-analytics.org/recall/Z-1281-2022. Source: US FDA. Licensed CC0.

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