Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000168) due to potential contamination risks. Affected units may have a low dead space design that could cause injection errors.
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 injection errors if used improperly.
The syringes have a low dead space design that could cause injection errors if not properly filled. This design may lead to inaccurate dosing or incomplete medication delivery during procedures.
Healthcare professionals using CustomEyes Procedure Packs with specific syringe models are most at risk. Patients receiving injections with these syringes may experience errors.
Check for the Part Number 58000168 on the syringe packaging. The product was sold with UDI-DI 30886158009574 and Lot/Batch Number 6072077.
Look for Part Number 58000168 on the syringe packaging to identify affected units.
The recalled packs contain Sol-M Luer Lock and Luer Slip 1ml syringes with Part Number 58000168.
Check for Part Number 58000168 on the syringe packaging, UDI-DI 30886158009574, and Lot/Batch Number 6072077.
The recall does not specify a stop-use action, so you can continue using them if you verify they are not affected.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2799-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2799-2024 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.
