Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001634) 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 include Sol-M Luer Lock and Luer Slip 1ml syringes. These syringes have a low dead space design that could lead to inaccurate medication dosing if not used correctly.
The syringes have a low dead space design, which means small amounts of liquid can remain in the syringe after drawing medication. If the syringe is not properly cleared of this residual liquid before use, it could lead to inaccurate medication dosing.
Users of CustomEyes Procedure Packs containing the specific syringes (Part Number 58001634) are affected. Healthcare professionals and patients using these packs for injections may be at risk of inaccurate dosing.
Check for the Part Number 58001634 on the syringe packaging. The product was sold with UDI-DI: 30886158031698 and Lot/Batch Number 6073601.
Look for the Part Number 58001634 on the syringe packaging to confirm if the product is affected.
The affected syringes have Part Number 58001634.
Check for the Part Number 58001634 on the syringe packaging. The product was sold with UDI-DI: 30886158031698 and Lot/Batch Number 6073601.
The recall does not specify a stop-use instruction, but you should check if your syringes have the Part Number 58001634 before use.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2895-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2895-2024 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.
