Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 584643) due to potential low dead space issues. 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 specific syringes from Sol-M. These syringes have a low dead space design that could lead to inaccurate dosing if used incorrectly.
The syringes have a low dead space design that can cause inaccurate dosing if used improperly. This means the actual amount of medication delivered might differ from what's intended, potentially leading to incorrect treatment.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving treatments with these syringes may experience inaccurate dosing.
Check for the Part Number 584643 on the syringe packaging. The product was sold with UDI-DI 30886158141717 and Lot/Batch Number 6068270.
Look for the Part Number 584643 on the syringe packaging to identify affected units.
The recall is due to low dead space syringes that could cause inaccurate dosing if used improperly.
Check the syringe packaging for Part Number 584643 to determine if they are affected. If so, stop using them and contact Beaver Visitec for further instructions.
The low dead space design may lead to inaccurate dosing, but the recall is for low risk as the hazard does not cause serious injury in normal use.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2788-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2788-2024 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.
