Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001609) due to potential low dead space risks. 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 medication dosing if used incorrectly.
The syringes have a low dead space design that can cause inaccurate medication dosing if not properly filled. This may lead to underdosing or overdosing depending on the medication and usage.
Users of CustomEyes Procedure Packs with the specified syringes, particularly healthcare professionals administering medications. Patients receiving treatments via these packs may be at risk of incorrect dosing.
Check for the Part Number 58001609 on the syringe packaging. The product was sold with UDI-DI: 30886158031544 and Lot/Batch Number 6064451.
Look for the Part Number 58001609 on the syringe packaging or the CustomEyes Procedure Pack label.
The recalled product contains Sol-M Luer Lock and Luer Slip 1ml syringes with Part Number 58001609.
The low dead space design could lead to inaccurate medication dosing if not properly filled, potentially causing underdosing or overdosing.
Check for the Part Number 58001609 on the syringe packaging or the CustomEyes Procedure Pack label.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2890-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2890-2024 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.
