Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M syringes (part 58001174) due to potential low dead space causing inaccurate dosing. Affected units sold with specific part numbers.
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 58001174) because these syringes have a low dead space that could lead to inaccurate medication dosing. This recall is important for medical users who might be administering medications with these syringes.
The syringes have a low dead space, meaning small amounts of liquid may remain in the syringe after withdrawal. This could lead to inaccurate medication dosing if the user doesn't account for the residual liquid. The risk is low but requires careful use to avoid medication errors.
Medical professionals and patients using CustomEyes Procedure Packs with the specific syringes (part number 58001174) are affected. Those administering medications with these syringes face the lowest risk of inaccurate dosing.
Check for the part number 58001174 on the syringe packaging or label. The product was sold with specific lot/batch numbers including 6068288. Look for the UDI-DI code 30886158022474 on the packaging.
Look for part number 58001174 on the syringe packaging or label to confirm if the product is affected.
The part number for the affected syringes is 58001174.
Check for part number 58001174 on the syringe packaging or label. The product was sold with specific lot/batch numbers including 6068288.
The recall states a potential for inaccurate dosing due to low dead space, but no specific risk of serious injury is mentioned.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2849-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2849-2024 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.
