# FDA recall Z-2829-2024

> **Beaver Visitec International, Inc.** · Class II · device recall initiated 2024-07-26.

## Product

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000866;

## Reason for recall

Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millennium Medical (Sol-M), Inc. These syringes  manufactured by Sol-M are present in some of BVI CustomEyes Procedure Packs.

## Distribution

US Nationwide distribution.

## Key facts

- **Recall number:** Z-2829-2024
- **Recalling firm:** Beaver Visitec International, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2024-07-26
- **Report date:** 2024-09-04

- **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-2829-2024

## Citation

> AI Analytics. FDA recall Z-2829-2024. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/Z-2829-2024. Source: US FDA. Licensed CC0.

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