BVI CustomEyes Procedure Packs Recalled Due to Sol-M Syringe Issue
Beaver Visitec International is recalling BVI CustomEyes Procedure Packs containing specific Sol-M syringes due to a voluntary recall by the syringe manufacturer.
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 described as a voluntary recall by the syringe manufacturer with no reported illnesses or injuries in the source text, fitting the criteria for a voluntary precautionary recall.
Plain-English summary
Beaver Visitec International, Inc. is recalling BVI CustomEyes Procedure Packs, Part Number 58001467, that contain Sol-M Luer Lock and Luer Slip 1ml syringes. The recall involves 1,328 units distributed nationwide in the United States. The specific lot number is 6071209, and the UDI-DI is 30886158024409.
This recall is being conducted because Sol-Millennium Medical (Sol-M), Inc. is voluntarily recalling low dead space syringes and luer slip tip syringes. The Sol-M syringes are present in some of the BVI CustomEyes Procedure Packs.
Healthcare providers and consumers should stop using these specific procedure packs and contact the manufacturer for instructions on return or replacement. The source text does not report any illnesses or injuries associated with this recall.
The recalled product
- Product
- BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001467;
- Manufacturer
- Beaver Visitec International, Inc.
- Category
- Medical Device — Syringes
- Hazard
- Affected units
- 1,328
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: 58001467
- UDI-DI: 30886158024409
- Lot/Batch Number: 6071209
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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