Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 584630) due to potential low dead space risks. Affected units include specific batch numbers and lot codes.
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 584630) because these syringes have a low dead space design that could cause issues during medical procedures. This recall affects healthcare professionals using these packs for procedures requiring precise fluid measurement.
The syringes have a low dead space design, which means they can hold less fluid than intended. This could lead to inaccurate fluid measurements during medical procedures, potentially causing complications if not properly managed.
Healthcare professionals who use CustomEyes Procedure Packs with the specified syringes are most at risk. The recall targets specific batches and lot numbers produced by Sol-M.
Check for the Part Number 584630 on the syringe packaging. Affected units include specific batch numbers (Lot/Batch 6067412) and UDI-DI codes (30886158141557).
Look for the Part Number 584630 on the syringe packaging to identify affected units.
The specific part number is 584630.
The affected batch number is 6067412.
Check for the Part Number 584630 on the syringe packaging and look for the Lot/Batch Number 6067412 or UDI-DI code 30886158141557.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2787-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2787-2024 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.
