Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001200) due to potential contamination risks. Affected units may have a risk of infection from improper use.
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 could pose a contamination risk if used improperly, which might lead to infections.
The syringes in question have a low dead space design and luer slip tips. If not properly handled, they could allow contaminants to enter the syringe, potentially causing infections during medical procedures.
Users of CustomEyes Procedure Packs containing Sol-M syringes (Part Number 58001200) are affected. Healthcare professionals and medical facilities using these packs may be at higher risk.
Check for the Part Number 58001200 on the syringe packaging. Affected packs may also have the UDI-DI code 30886158022757 or Lot/Batch Number 6068518.
Look for the Part Number 58001200 on the syringe packaging or the UDI-DI code 30886158022757.
The recalled packs contain Sol-M Luer Lock and Luer Slip 1ml syringes with Part Number 58001200.
Check for the Part Number 58001200 on the syringe packaging or the UDI-DI code 30886158022757 or Lot/Batch Number 6068518.
The recall record does not specify a remedy, so contact Beaver Visitec for further instructions.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2852-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2852-2024 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.
