Beaver Visitec International, Inc. recalls BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584550;
- Recall date
- July 26, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- Z-2784-2024
- FDA classification
- Class II
- Brand / firm
- Beaver Visitec International, Inc.
- Sold / distributed
- US Nationwide distribution.
Why it was recalled
Data in RES.
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: 584550;
Get recall alerts
Free email alert whenever Beaver Visitec International, Inc. has a new recall — straight from official government data. Unsubscribe anytime.
More recalls from: Beaver Visitec International, Inc.