BVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Issue
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing Sol-M syringes due to a voluntary recall of the syringe components.
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 source text describes a voluntary recall of syringes without reporting any illnesses, injuries, or specific hazards, which aligns with the rubric for voluntary precautionary recalls.
Plain-English summary
Beaver Visitec International, Inc. is recalling BVI CustomEyes Procedure Packs, Part Number 58001014, that contain Sol-M Luer Lock and Luer Slip 1ml syringes. The recall involves 424 units distributed nationwide in the United States.
The recall is being conducted because Sol-Millennium Medical (Sol-M), Inc. is voluntarily recalling low dead space syringes and luer slip tip syringes. These specific syringes are present in some of the BVI CustomEyes Procedure Packs.
The source text does not specify the exact nature of the defect or the potential hazards associated with the Sol-M syringes. Consumers and healthcare providers should check their inventory for the affected Part Number 58001014 and Lot/Batch Numbers 6071020 and 6075094.
The recalled product
- Product
- BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001014;
- Manufacturer
- Beaver Visitec International, Inc.
- Category
- Medical Device — Syringes
- Hazard
- Affected units
- 424
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 (4)
- Part Number: 58001014
- UDI-DI: 30886158021729
- Lot/Batch Number: 6071020
- 6075094
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.
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