Recall Z-2800-2024— Beaver Visitec International, Inc.

Name: FDA recall Z-2800-2024
Creator: U.S. Food and Drug Administration
Published: 2024-07-26

Class II · Ongoing

Class II FDA medical device recall by Beaver Visitec International, Inc., initiated 2024-07-26. FDA's recall record names no specific 510(k) clearance for this event. Product: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000192;. Reason: 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..

Recalling firm: Beaver Visitec International, Inc.
Classification: Class II
Status: Ongoing
Initiated: 2024-07-26
Firm location: Waltham, MA, United States

Product description

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000192;

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.

Data sourced from openFDA. This site is unofficial and independent of the FDA.