Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000960) due to potential low dead space issues. Affected units sold with specific lot numbers.
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 58000960) because these syringes have a low dead space design that could cause issues during medical procedures. This recall matters because improper use of low dead space syringes may lead to inaccurate dosing or complications in medical treatments.
Low dead space syringes can cause inaccurate dosing if air is trapped inside the syringe during medical procedures. This may lead to incorrect medication delivery or complications in treatments requiring precise fluid measurements.
Medical professionals using CustomEyes Procedure Packs with the specific syringe part number 58000960 are likely affected. Patients receiving procedures using these syringes may also be at risk if the syringes are used incorrectly.
Check for the part number 58000960 on the syringe packaging. Affected units were sold with lot/batch number 6060636 and UDI-DI code 30886158022122.
Look for part number 58000960 on the syringe packaging or label.
The part number for the recalled syringes is 58000960.
The affected lot number is 6060636.
Check for part number 58000960 on the syringe packaging or label. Affected units were sold with lot/batch number 6060636 and UDI-DI code 30886158022122.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2834-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2834-2024 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.
