Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001608) 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 Sol-M Luer Lock and Luer Slip 1ml syringes. These syringes have a low dead space design that could lead to inaccurate dosing if used incorrectly, potentially causing medication errors.
The syringes have a low dead space design, which means small amounts of liquid may remain in the syringe after drawing medication. This could lead to inaccurate dosing if the user doesn't properly expel the liquid before administering the dose.
Users of CustomEyes Procedure Packs containing Sol-M syringes (Part Number 58001608) are affected. Healthcare professionals and patients using these packs for injections are most at risk of medication errors.
Check for the Part Number 58001608 on the syringe packaging. The product was sold with UDI-DI: 30886158031537 and Lot/Batch Number 6067129.
Look for the Part Number 58001608 on the syringe packaging or the CustomEyes Procedure Pack label.
The recall includes Sol-M Luer Lock and Luer Slip 1ml syringes with Part Number 58001608.
Check for the Part Number 58001608 on the syringe packaging or the CustomEyes Procedure Pack label. The product also has UDI-DI: 30886158031537 and Lot/Batch Number 6067129.
The recall does not specify a remedy, so you should check with the manufacturer for guidance on safe handling or disposal.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2889-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2889-2024 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.
