BVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Issue
Beaver Visitec International is recalling 44 units of BVI CustomEyes Procedure Packs because they contain syringes from Sol-Millennium Medical, which are subject to a separate voluntary recall.
What this means for you
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Our severity reasoning: The recall is classified as FDA Class II, but the source text explicitly describes it as a 'voluntary recall' and does not report any injuries, illnesses, or specific hazards, fitting the criteria for a voluntary precautionary recall.
Plain-English summary
Beaver Visitec International, Inc. is voluntarily recalling 44 units of BVI CustomEyes Procedure Packs, Part Number 58001699. These specific packs contain Sol-M Luer Lock and Luer Slip 1ml syringes manufactured by Sol-Millennium Medical (Sol-M), Inc.
The recall is being conducted because the Sol-M syringes included in these packs are subject to a separate voluntary recall by the manufacturer. The source text does not specify the exact nature of the defect or hazard associated with the Sol-M syringes, nor does it report any injuries or illnesses.
The affected products were distributed nationwide in the United States. Healthcare facilities and distributors should identify and quarantine the affected units, specifically those with Part Number 58001699, UDI-DI 30886158031964, and Lot/Batch Number 6071000. Users should stop using these specific procedure packs and contact the recalling firm for instructions on return or disposal.
The recalled product
- Product
- BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001699;
- Manufacturer
- Beaver Visitec International, Inc.
- Category
- Medical Device — Syringes
- Hazard
- Affected units
- 44
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (3)
- Part Number: 58001699
- UDI-DI: 30886158031964
- Lot/Batch Number: 6071000
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 159 recalled by Beaver Visitec International, Inc. under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 159 products in this recall →Related recalls
Same manufacturer · Beaver Visitec International, Inc.
See all →- ModerateLaser and endoscopy systems recalled over ferrites omitted from a USB cable
FDA (Devices) · 2026-01-07
- ModerateBVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringes
FDA (Devices) · 2024-09-04
- ModerateBVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Issue
FDA (Devices) · 2024-09-04
- ModerateBVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Issue
FDA (Devices) · 2024-09-04
- ModerateBVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Issue
FDA (Devices) · 2024-09-04
Same hazard · defective component
See all →- HighBeckman Coulter Sample Probes with Defective Tips Clinical Chemistry
FDA (Devices) · 2025-06-11
- SevereMedline Medical Convenience Kits Recalled for Defective Endotracheal Tubes
FDA (Devices) · 2025-04-16
- SevereMedline Medical Procedure Kits with Medtronic Aortic Cannula Recalled
FDA (Devices) · 2025-04-16
- SevereExactech AcuMatch XLE Hip Implant Liner Recall
FDA (Devices) · 2025-02-19
- HighMEDLINE Surgical Convenience Kits Recalled for Defective Smoke Evacuation Component
FDA (Devices) · 2024-12-11