Beaver Visitec International, Inc. recalls BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001970;

Recall date

July 26, 2024

Source

U.S. Food & Drug Administration (FDA) — enforcement report

Recall number

Z-2930-2024

FDA classification

Class II

Brand / firm

Beaver Visitec International, Inc.

Sold / distributed

US Nationwide distribution.

Why it was recalled

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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001970;