FDA Medical Device Recalls (openFDA)
Beaver Visitec International, Inc.: BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000056;
- Recall number
- Z-2795-2024
- Recalling firm
- Beaver Visitec International, Inc.
- Product
- BVI CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes, Part Number: 58000056;
- Status
- Open, Classified
- Initiated
- 2024-07-26
- Posted
- 2024-08-28
- Terminated
- not on file
- 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.
- Root cause
- No Marketing Application
- 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 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.
- Quantity
- 198 units
- Distribution
- US Nationwide distribution.
- Lot, serial or model codes
- Part Number: 58000056; UDI-DI: 30886158008980; Lot/Batch Number: 6065306, 6069372
- 510(k) numbers
- not on file
- PMA numbers
- not on file
- Product code
- KDD
- Firm FEI
- 1211998
- Firm city
- Waltham
- Firm state
- MA
- Firm country
- not on file
Where this comes from
- Register
- FDA Medical Device Recalls (openFDA)
- Publisher
- U.S. Food and Drug Administration (openFDA)
- File
- device-recall-0001-of-0001.json.zip
- sha256
- b87518bfe2e8
- Size
- 288210821 bytes
- Published
- 2026-09-28
- Read
- 2026-09-29T08:25:23.626Z
- Source file
- Source file retained · verify
- Refresh due
- 2026-10-06
Unless otherwise noted, the content, data, documentation, code, and related materials on openFDA is public domain and made available with a Creative Commons CC0 1.0 Universal dedication.
Cite as
FDA Medical Device Recalls (openFDA) (U.S. Food and Drug Administration (openFDA)), device-recall-0001-of-0001.json.zip, sha256 b87518bfe2e8, published 2026-09-28