Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000477) 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 improper medication delivery or dosing issues during procedures.
Healthcare 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 58000477 on the syringe packaging. The recall affects CustomEyes Procedure Packs sold with Sol-M Luer Lock and Luer Slip 1ml syringes.
Look for the Part Number 58000477 on the syringe packaging to identify affected units.
The recall is for syringes with a low dead space design that could cause injection errors if used incorrectly.
Check for the Part Number 58000477 on the syringe packaging. The recall affects CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes.
The official recall notice does not specify a remedy or action steps beyond checking the syringe packaging.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2809-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2809-2024 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.
