Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001695) due to potential low dead space risks. Affected units sold with specific lot 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 cause inaccurate 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 dosing if the syringe is not properly cleared before use.
Users of CustomEyes Procedure Packs with the specific syringe part number 58001695 are affected. Healthcare professionals and patients using these syringes for medical procedures are most at risk.
Check for the part number 58001695 on the syringe packaging. The recall includes CustomEyes Procedure Packs sold with these specific syringes, which have a UDI-DI code 30886158031957 and lot number 6062796.
Look for the part number 58001695 on the syringe packaging to confirm if it is affected.
The part number for the recalled syringes is 58001695.
Check for the part number 58001695 on the syringe packaging. Affected packs also have UDI-DI code 30886158031957 and lot number 6062796.
The official recall does not mention a fix; affected units should be checked and discarded if confirmed.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2902-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2902-2024 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.
