Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001637) due to potential low dead space issues. Affected units may cause inaccurate dosing if used improperly.
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.
Beaver Visitec is recalling CustomEyes Procedure Packs that contain Sol-M Luer Lock and Luer Slip 1ml syringes. These syringes have a low dead space design that could lead to inaccurate dosing if used incorrectly, potentially causing medication errors.
The syringes have a low dead space design, meaning small amounts of liquid may remain in the syringe after drawing medication. If the syringe is not properly resealed or used, this could lead to inaccurate dosing when administering medication.
Users of CustomEyes Procedure Packs containing Sol-M syringes (Part Number 58001637) are affected. Healthcare professionals and patients using these packs for injections are most at risk of medication errors.
Check for the Part Number 58001637 on the syringe packaging. The product was sold with UDI-DI: 30886158031858 and Lot/Batch Number 6064640. These packs are used for medical procedures involving injections.
Look for the Part Number 58001637 on the syringe packaging to identify affected units.
The Part Number for the recalled syringes is 58001637.
Check for the Part Number 58001637 on the syringe packaging or look for the UDI-DI: 30886158031858 and Lot/Batch Number 6064640.
The recall does not specify a remedy, so contact Beaver Visitec for guidance on next steps.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2897-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2897-2024 from Beaver Visitec. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
