FDA Recall Open, Classified

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58002075;

Recall: Z-2937-2024 · Initiated July 26, 2024

Recall

Recall Number
Z-2937-2024
Event Number
95068
Firm
Beaver Visitec International, Inc.
FEI Number
1211998
Product Code
KDD
Status
Open, Classified
Root Cause
No Marketing Application
Initiated
July 26, 2024
Posted
August 28, 2024
Address
500 Totten Pond Rd, 10, City Point Waltham, MA, 02451-1916

Description

BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58002075;

Reason

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.

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.

Distribution

US Nationwide distribution.

Quantity

56 units