BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer… — Class II medical device recall Z-2896-2024
Ongoing recall by Beaver Visitec International, Inc., reported 2024-09-04, distributed nationwide. Due to a voluntary recall of low dead space syringes, and luer slip tip syringes manufactured by Sol-Millenniu
| Recall number | Z-2896-2024 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Beaver Visitec International, Inc., Waltham, MA, United States |
| Recall initiated | 2024-07-26 |
| Classified | 2024-08-28 |
| Reported by FDA | 2024-09-04 |
| Distributed | Nationwide (US) |
| Quantity | 444 units |
| UPC / GTIN / UDI-DI | 30886158031681 |
| Lot numbers | 6063185, 6067384 |
| Model numbers | 58001635 |
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001635;
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-2896-2024. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.