BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58001014;
FDA Recall Z-2836-2024 · Posted 2024-08-28
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Recalling FirmBeaver Visitec International, Inc.
Recall StatusOpen, Classified
Product CodeKDD
Date Initiated2024-07-26
Product Quantity424 units
Reason for Recall
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.
Firm Action
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 [email protected]. 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
[email protected] 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.
Root Cause
No Marketing Application
Distribution Pattern
US Nationwide distribution.
Official Source
View FDA Recall →Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.
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