Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000120) 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 dosing if used incorrectly, potentially causing medication errors.
The syringes have a low dead space design, meaning small amounts of liquid can remain in the syringe after use. This could lead to inaccurate dosing if the liquid is not properly expelled before administering medication.
Healthcare professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving treatments with these syringes may also be affected if the dosing is inaccurate.
Check for the Part Number 58000120 on the syringe packaging. The product was sold with UDI-DI: 30886158009512 and Lot/Batch Number 6071452.
Look for the Part Number 58000120 on the syringe packaging to identify affected units.
The syringes have a low dead space design that could lead to inaccurate dosing if not properly emptied before use.
Check for the Part Number 58000120 on the syringe packaging. The product was sold with UDI-DI: 30886158009512 and Lot/Batch Number 6071452.
The recall does not require immediate stop use; affected units should be checked for the Part Number 58000120.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2796-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2796-2024 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.
