Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000985) due to potential contamination risks. Affected units sold with specific part numbers and batch codes.
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 may have a low dead space design that could lead to contamination during medical procedures.
The syringes have a low dead space design, which means small amounts of fluid may remain in the syringe after use. This could potentially lead to contamination if not properly cleaned or handled during medical procedures.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving procedures using these syringes could also be affected.
Check for the part number 58000985 on the syringe packaging. Affected packs also have UDI-DI: 30886158021460 and lot/batch number 6072192.
Look for part number 58000985 on the syringe packaging or the CustomEyes Procedure Pack label.
The recalled packs contain Sol-M Luer Lock and Luer Slip 1ml syringes with part number 58000985.
Check for part number 58000985 on the syringe packaging or the CustomEyes Procedure Pack label. Also look for UDI-DI: 30886158021460 and lot/batch number 6072192.
The recall record does not specify a remedy, so contact Beaver Visitec for further instructions.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2835-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2835-2024 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.
