Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001624) 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 recalls CustomEyes Procedure Packs containing specific Sol-M syringes because they have low dead space that could lead to inaccurate dosing. This affects medical users who might be at risk of incorrect medication amounts.
The syringes have low dead space, meaning small amounts of fluid can remain in the syringe after use. This could cause inaccurate dosing if the fluid isn't fully expelled before administering medication.
Medical professionals and patients using CustomEyes Procedure Packs with the recalled syringes. Those most at risk are users who rely on precise dosing for medications.
Check for the Part Number 58001624 or 58001622 on the syringe packaging. The product was sold with UDI-DI: 30886158031865 and Lot/Batch Number 6064651.
Look for Part Numbers 58001624 or 58001622 on the syringe packaging to identify affected units.
The syringes have low dead space, which could lead to inaccurate dosing if not properly emptied before medication administration.
Check for Part Numbers 58001624 or 58001622 on the syringe packaging, or look for UDI-DI: 30886158031865 and Lot/Batch Number 6064651.
The recall does not require immediate discontinuation; users should check if their syringes are affected before taking action.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2892-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2892-2024 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.
