Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000508) due to potential low dead space issues. Affected units may cause inaccurate dosing if used improperly.
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 dosing if used incorrectly, potentially causing medication errors.
The syringes have a low dead space design, meaning small amounts of fluid can remain in the syringe after drawing medication. If the syringe is not properly cleared of this fluid before use, it could lead to inaccurate dosing of medication.
Users of CustomEyes Procedure Packs with the specific syringe part number 58000508 are affected. Healthcare professionals and patients using these syringes for medical procedures are most at risk of inaccurate dosing.
Check for the part number 58000508 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 58000508 on the syringe packaging to confirm if the product is affected.
The recall is due to low dead space syringes that could lead to inaccurate dosing if not properly cleared of residual fluid before use.
The official recall notice does not specify a remedy or action for affected products.
The potential risk is inaccurate dosing due to low dead space design, which could lead to medication errors if not properly cleared.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2812-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2812-2024 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.
