Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58002000) due to potential low dead space causing inaccurate dosing. Affected units sold with specific part numbers and batch codes.
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 (Part Number 58002000) because these syringes have a low dead space that could lead to inaccurate medication dosing. This recall affects healthcare professionals using these syringes for medical procedures.
The syringes have a low dead space, which means small amounts of liquid can remain in the syringe after drawing medication. This could cause inaccurate dosing if the liquid is not properly accounted for during medical procedures.
Healthcare professionals who use CustomEyes Procedure Packs containing the specific 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 58002000 on the syringe packaging. Affected packs also have UDI-DI: 30886158034026 and Lot/Batch Number 6071764.
Look for Part Number 58002000 on the syringe packaging or the CustomEyes Procedure Pack label.
The recall is due to low dead space syringes that could lead to inaccurate medication dosing during medical procedures.
The official recall notice does not specify a remedy or action steps beyond checking product details.
Check for Part Number 58002000, UDI-DI: 30886158034026, and Lot/Batch Number 6071764 on the syringe packaging.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2933-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2933-2024 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.
