Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001019) due to potential low dead space causing inaccurate dosing. Affected units include specific lot numbers and batch dates.
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 medication dosing if used improperly.
The syringes have a low dead space design, which means small amounts of liquid may remain in the syringe after use. This could lead to inaccurate medication dosing if the syringe is not properly cleared before administering the medication.
Users of CustomEyes Procedure Packs containing the specified syringes are affected. Healthcare professionals and patients using these packs for medical procedures are most at risk.
Check for the Part Number 58001019 on the syringe packaging. Affected units include specific lot numbers: 6069184, 6069624, and 6075235.
Look for the Part Number 58001019 on the syringe packaging to identify affected units.
The recalled packs contain Sol-M Luer Lock and Luer Slip 1ml syringes with Part Number 58001019.
Affected lot numbers are 6069184, 6069624, and 6075235.
Check for the Part Number 58001019 on the syringe packaging and verify the lot numbers listed.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2837-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2837-2024 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.
