Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58002063) due to potential contamination risks. Affected units may have a low dead space design that could cause injection errors.
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 injection errors if used improperly.
The syringes have a low dead space design that could cause injection errors if not used correctly. This design may lead to inaccurate dosing or incomplete medication delivery during procedures.
Medical professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients receiving injections with these syringes may experience errors.
Check for the Part Number 58002063 on the syringe packaging. The syringes are part of CustomEyes Procedure Packs sold by Beaver Visitec.
Look for the Part Number 58002063 on the syringe packaging to identify affected units.
The recall is due to a low dead space design in the syringes that could cause injection errors if used improperly.
Check the syringe packaging for the Part Number 58002063. If it matches, contact Beaver Visitec for guidance.
The low dead space design may lead to inaccurate dosing or incomplete medication delivery during procedures.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2935-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2935-2024 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.
