Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (part 58002074) due to potential low dead space causing inaccurate dosing. Affected units sold with specific part numbers and batch codes.
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 cause inaccurate dosing if the syringe is not properly cleared before administering medication.
Users of CustomEyes Procedure Packs containing the specified syringes are affected. Healthcare professionals and patients using these packs for medical procedures are most at risk.
Check for the part number 58002074 on the syringe packaging. The product was sold with specific batch numbers and lot codes including 6074312.
Look for the part number 58002074 on the syringe packaging to identify affected units.
The part number is 58002074.
The affected batch number is 6074312.
Check for the part number 58002074 on the syringe packaging or look for the batch number 6074312.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2936-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2936-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
