Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (part 58001836) 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 fluid can remain in the syringe after drawing medication. This could cause inaccurate dosing if the user does not properly expel all fluid before administering the medication.
Users of CustomEyes Procedure Packs with specific part numbers (58001836 and 58001835) are affected. Healthcare professionals using these syringes for injections may be at risk of inaccurate dosing.
Check for part numbers 58001836 or 58001835 on the syringe packaging. The lot/batch number 6066752 is also associated with these recalled units.
Look for part numbers 58001836 or 58001835 on the syringe packaging or the CustomEyes Procedure Pack label.
Part numbers 58001836 and 58001835 are affected.
Check for part numbers 58001836 or 58001835 on the syringe packaging or the CustomEyes Procedure Pack label.
The recall does not specify a remedy, so contact Beaver Visitec for further instructions.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2918-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2918-2024 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.
