Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (part 58001527) 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 medication dosing if used incorrectly.
The syringes have a low dead space design, meaning small amounts of liquid can remain in the syringe after drawing medication. This could lead to inaccurate dosing if the user doesn't properly expel the liquid before administering the dose.
Users of CustomEyes Procedure Packs with Sol-M syringes (part number 58001527) are affected. Healthcare professionals and patients using these packs for injections are most at risk.
Check for the part number 58001527 on the syringe packaging. The product was sold with specific lot/batch numbers (6071514) and UDI-DI code 30886158031483.
Look for the part number 58001527 on the syringe packaging or the product label.
The part number is 58001527.
The recall is due to low dead space syringes that could lead to inaccurate medication dosing if not used properly.
Yes, the low dead space design could cause inaccurate dosing if the user doesn't properly expel the liquid before administering the dose.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2881-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2881-2024 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.
