Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001123) due to potential low dead space causing injection errors.
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 specific syringes from Sol-M. These syringes have a low dead space design that could cause injection errors if used improperly.
The syringes have a low dead space design that could lead to injection errors if not properly used. This design may cause medication to not be fully expelled from the syringe before injection, potentially affecting treatment.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving injections with these syringes may experience errors.
Check for CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes. The part number is 58001123, and the lot numbers are 6047610, 6049448, or 6050478.
Look for the part number 58001123 on the syringes or the CustomEyes Procedure Pack.
The recall is due to low dead space syringes that could cause injection errors if not properly used.
Check the part number and lot numbers to see if your syringes are affected. If they are, contact Beaver Visitec for instructions.
The low dead space design could lead to injection errors, but the risk is low if used correctly.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2846-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2846-2024 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.
