Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000867) due to potential low dead space causing inaccurate dosing. Affected units sold with specific batch 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. 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 that could cause inaccurate medication dosing if not properly filled. This might lead to under-dosing or over-dosing depending on the medication and the user's technique.
Users of CustomEyes Procedure Packs containing the specified syringes, particularly healthcare professionals administering medications. Patients receiving treatments with these syringes may be at risk of incorrect dosing.
Check for the Part Number 58000867 on the syringe packaging. Affected packs were sold with batch numbers 6054595, 6064075, 6071826, or 6075095.
Look for the Part Number 58000867 on the syringe packaging to identify affected units.
The recalled packs contain Sol-M Luer Lock and Luer Slip 1ml syringes with Part Number 58000867.
Affected batch numbers are 6054595, 6064075, 6071826, and 6075095.
Check the syringe packaging for Part Number 58000867 and the specific batch 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-2830-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2830-2024 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.
