Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M syringes (part 58000426) due to potential low dead space causing inaccurate dosing. Affected units include specific lot numbers and UDI-DI 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 (part number 58000426) because these syringes have a low dead space that could lead to inaccurate dosing during medical procedures. This recall is important because improper dosing could affect treatment outcomes.
The syringes have a low dead space, which means small amounts of fluid may remain in the syringe after drawing medication. This could lead to inaccurate dosing if the fluid is not properly accounted for during medical procedures.
Medical professionals using CustomEyes Procedure Packs with the specific syringe part number 58000426 are most at risk. Patients receiving treatments with these syringes may also be affected.
Check for the part number 58000426 on the syringe packaging. Affected units also have UDI-DI code 30886158019894 and lot/batch number 6069170.
Look for part number 58000426 on the syringe packaging or label.
The recall is due to low dead space syringes that could lead to inaccurate dosing during medical procedures.
Check the syringe packaging for part number 58000426. If you have it, contact Beaver Visitec for guidance.
The low dead space could cause inaccurate dosing, but the recall is for low-risk correction to ensure proper medication delivery.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2807-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2807-2024 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.
