Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (part 58001711) due to potential air embolism risk. Affected units sold with specific lot 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. These syringes could cause air embolism if used improperly, which is a serious medical risk.
The syringes have a design that may allow air to enter the bloodstream during injections, potentially causing air embolism. This is a serious medical condition that can be life-threatening if not detected early.
Healthcare professionals using CustomEyes Procedure Packs with the specific syringe part numbers are most at risk. Patients receiving procedures with these syringes could face air embolism.
Check for CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (part number 58001711). Affected units have lot numbers 6070885 or 6074819.
Look for part number 58001711 on the syringes in the CustomEyes Procedure Packs.
Reach out to Beaver Visitec for guidance on whether your specific pack is affected.
The recalled packs contain Sol-M Luer Lock and Luer Slip 1ml syringes with part number 58001711.
Check for part number 58001711 on the syringes and lot numbers 6070885 or 6074819.
The recall does not require immediate stop use; contact Beaver Visitec to determine if your specific pack is 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-2905-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2905-2024 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.
