Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000711) 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 specific syringes from Sol-M. These syringes have a low dead space design that could lead to inaccurate medication dosing if used incorrectly.
The syringes have a low dead space design, which means small amounts of liquid may remain in the syringe after use. If not properly accounted for, this could lead to inaccurate medication dosing during administration.
Users of CustomEyes Procedure Packs with the specified syringes, particularly healthcare professionals administering medications. Patients receiving treatments using these packs are at minimal risk if the syringes are used correctly.
Check for the Part Number 58000711 on the syringe packaging. The recall applies to CustomEyes Procedure Packs sold with these specific syringes, which may have been distributed through medical suppliers.
Look for the Part Number 58000711 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 medication dosing if used incorrectly.
Check for the Part Number 58000711 on the syringe packaging. The recall applies to CustomEyes Procedure Packs with these specific syringes.
The recall record does not specify a remedy, so contact the manufacturer directly for guidance.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2819-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2819-2024 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.
