CustomEyes Procedure Packs (Beaver Visitec) – Syringe Recall (2024)
Hazard assessment based on recall description.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 584003;
Brand
Beaver Visitec International, Inc.
Lot Codes / Batch Numbers
Part Number: 584003, UDI-DI: 30886158141496, Lot/Batch Number: 6063717
Products Sold
Part Number: 584003; UDI-DI: 30886158141496; Lot/Batch Number: 6063717
Beaver Visitec International, Inc. is recalling BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 5 due to 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 m. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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.
Recommended Action
Per FDA guidance
On July 27, 2024 URGENT FIELD SAFETY NOTICE letters were sent to consignees. Actions required of you 1. Please immediately determine if any of the affected CustomEyes Procedure Packs are within your facility. In such case, quarantine them, and discontinue use until correct recall labels are applied. Please refer to Appendix 1 CustomEyes Procedure Packs List 2. If you have further distributed this product, please notify your customers by initiating a subrecall. Consider all potential users of this product in your user supply chain. You are encouraged to use a copy of this recall notification letter when contacting your customers. 3. Please follow the attached instructions for placing the recall labels on the products containing Sol-M syringes, which inform the users to not use the affected syringes. If additional recall labels are needed, contact bvi2958@sedgwick.com. Product may be returned to inventory once properly over-labeled. Refer to Appendix 2 Over labeling Instructions 4. At the point of clinical use, the Sol-M syringes are to be discarded. Photographs of Sol-M syringes are enclosed to assist in identification. Appendix 3 Images 5. Ensure that appropriate personnel within your organization are made aware of this field action 6. To maintain awareness, we suggest to post this URGENT MEDICAL DEVICE RECALL NOTICE and Sol-M syringe photographs on or near the affected products in your inventory location 7. Please fill out, scan and email the completed Business Response Form to BVI Sedgwick at bvi2958@sedgwick.com within seven (7) days BVI is committed to providing high quality products to you and apologizes for any inconvenience this field action may cause. If you have any questions, please reach out to your Sales Representative.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026