Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58001054) due to potential contamination risks. Affected units may have a UDI-DI code 30886158022078 or batch 6071307.
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 pose contamination risks if used improperly, though the recall is voluntary and not linked to specific injuries.
The syringes were manufactured by Sol-M and may contain contaminants due to a low dead space design. This could lead to infections or other issues if the syringes are not properly sterilized before use.
Healthcare professionals using CustomEyes Procedure Packs with the specified syringes are most at risk. Patients using these packs may also be affected if the syringes are used incorrectly.
Check for the Part Number 58001054 on the syringe packaging. Affected packs also have a UDI-DI code 30886158022078 or batch number 6071307.
Look for the Part Number 58001054 or UDI-DI code 30886158022078 on the syringe packaging.
Beaver Visitec recalls CustomEyes Procedure Packs containing Sol-M Luer Lock and Luer Slip 1ml syringes due to potential contamination risks from the low dead space design.
Check for the Part Number 58001054 or UDI-DI code 30886158022078 on the syringe packaging. Affected packs also have a batch number of 6071307.
The recall is for potential contamination risks, but no specific injuries have been reported. The hazard level is low risk.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2841-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2841-2024 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.
