Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M syringes (part 58001138) due to potential low dead space causing inaccurate dosing. Affected users should check product details.
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 medication dosing if used improperly.
The syringes have a low dead space design, which means small amounts of liquid may remain in the syringe after use. This could lead to inaccurate medication dosing if the user doesn't account for the residual liquid.
Users of CustomEyes Procedure Packs containing Sol-M syringes (part number 58001138) are affected. Healthcare professionals and patients using these syringes for medical procedures are most at risk.
Check for the part number 58001138 on the syringe packaging. The product was sold with UDI-DI: 30886158022320 and lot number 6064069.
Look for part number 58001138 on the syringe packaging or the CustomEyes Procedure Pack label.
The part number is 58001138.
Check for part number 58001138 on the syringe packaging or the CustomEyes Procedure Pack label.
The recall does not mention a fix or remedy; users should check if they have the recalled product and contact the manufacturer if needed.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2847-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2847-2024 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.
