Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M syringes (part 58001526) due to potential low dead space risks. 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 Sol-M Luer Lock and Luer Slip 1ml syringes (part number 58001526) because these syringes have a low dead space that could lead to inaccurate dosing if used incorrectly. This recall affects medical professionals and patients using these syringes for procedures.
The syringes have a low dead space, meaning small amounts of fluid can remain in the syringe after drawing liquid. If the syringe is not properly cleared of this residual fluid before use, it could lead to inaccurate dosing of medications or solutions.
Medical professionals and patients who use the CustomEyes Procedure Packs with the specified syringes are likely affected. Those using the syringes for procedures where precise dosing is critical are at higher risk.
Check for the part number 58001526 on the syringe packaging or label. The syringes are part of Beaver Visitec's CustomEyes Procedure Packs sold with the UDI-DI: 30886158031476 and lot number 6070130.
Look for the part number 58001526 on the syringe packaging or label to confirm if the product is affected.
The part number is 58001526.
Check for the part number 58001526 on the syringe packaging or label. The syringes are part of Beaver Visitec's CustomEyes Procedure Packs with UDI-DI: 30886158031476 and lot number 6070130.
The recall does not require immediate stop use; check the part number to confirm if affected.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2880-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2880-2024 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.
