Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 584545) due to potential low dead space issues. Affected units may cause inaccurate measurements during medical procedures.
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 specific syringes from Sol-M. These syringes have a low dead space design that could lead to inaccurate fluid measurements during medical procedures, which might affect treatment outcomes.
The syringes have a low dead space design, meaning small amounts of fluid can remain in the syringe after use. This could lead to inaccurate fluid measurements during medical procedures, potentially affecting treatment effectiveness.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving procedures with these syringes may also be affected if the measurements are inaccurate.
Check for the Part Number 584545 on the syringe packaging. The recall includes CustomEyes Procedure Packs that contain Sol-M Luer Lock and Luer Slip 1ml syringes.
Look for the Part Number 584545 on the syringe packaging to identify affected units.
The recall is due to potential low dead space in the syringes, which could lead to inaccurate fluid measurements during medical procedures.
Check for the Part Number 584545 on the syringe packaging. The recall includes CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes.
The recall record does not specify a remedy, so check with the manufacturer 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-2783-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2783-2024 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.
