Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M syringes (part 58001110) due to potential low dead space risks. 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 harmful medication levels.
The syringes have a low dead space design, meaning small amounts of liquid can remain in the syringe after drawing medication. If the user does not properly account for this residual liquid, they might administer too little medication, leading to ineffective treatment.
Users of CustomEyes Procedure Packs with Sol-M syringes (part number 58001110) are affected. Healthcare professionals and patients using these syringes for injections may be at risk if the low dead space causes inaccurate dosing.
Check for the part number 58001110 on the syringe packaging. The product was sold with specific lot/batch numbers (6073585) and UDI-DI code 30886158022177.
Look for part number 58001110 on the syringe packaging to confirm if the product is affected.
The recall is due to low dead space syringes that could lead to inaccurate dosing if not used properly.
Check the syringe packaging for part number 58001110. If affected, contact Beaver Visitec for guidance.
The low dead space design could cause inaccurate dosing if the user does not account for residual liquid, but the risk is low and not immediately dangerous.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2843-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2843-2024 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.
