BVI CustomEyes Procedure Packs Recalled for Sol-M Syringe Components
Beaver Visitec International is voluntarily recalling BVI CustomEyes Procedure Packs containing Sol-M syringes. Approximately 79 units were distributed nationwide with no reported injuries.
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: This is a voluntary FDA Class II recall with no reported illnesses or injuries. The source material does not specify the underlying safety hazard, characterizing this as a precautionary recall with limited detail about the actual risk.
Plain-English summary
Beaver Visitec International, Inc. is voluntarily recalling BVI CustomEyes Procedure Packs (Part Number 58001865) that contain syringes manufactured by Sol-Millennium Medical, Inc. The recalled syringes include low dead space models and luer slip tip models.
The recall affects approximately 79 units distributed nationwide. The affected product can be identified by Part Number 58001865, UDI-DI 30886158033166, and Lot Number 6069158. No illnesses or injuries have been reported in association with this recall.
Healthcare providers and facilities that have received these procedure packs should discontinue use of the affected syringes. Those with questions may contact Beaver Visitec International, Inc. or the FDA. This Class II recall has been assigned FDA recall number Z-2921-2024.
The recalled product
- Product
- BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001865;
- Manufacturer
- Beaver Visitec International, Inc.
- Hazard
- syringe-defect
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: 58001865
- UDI-DI: 30886158033166
- Lot/Batch Number: 6069158
Distribution
Distributed nationwide across the United States.
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