Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001025) 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 58001025) because these syringes have a low dead space design that could cause inaccurate dosing. This recall affects medical professionals and patients using these syringes for procedures.
The syringes have a low dead space design, which means small amounts of fluid can remain in the syringe after drawing. This could lead to inaccurate dosing when administering medication or fluids, potentially causing underdosing or overdosing in medical procedures.
Medical professionals and patients who use CustomEyes Procedure Packs with the specified syringes are affected. Those using the recalled syringes for procedures are at higher risk due to potential dosing inaccuracies.
Check for CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part Number 58001025). The lot number is 6064450 and the UDI-DI is 30886158021637.
Look for the Part Number 58001025 on the syringe packaging or label.
The recall is due to low dead space syringes that could cause inaccurate dosing during medical procedures.
The official recall notice does not specify a remedy or action steps for affected products.
Check for the Part Number 58001025 on the syringe packaging or label. The lot number is 6064450 and the UDI-DI is 30886158021637.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2839-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2839-2024 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.
