Beaver Visitec recalls CustomEyes Procedure Packs with Sol-M Luer Lock and Luer Slip 1ml syringes (Part 58000192) due to potential low dead space causing inaccurate dosing. Affected units sold with specific part numbers and batch 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. These syringes have a low dead space design that could lead to inaccurate medication dosing if used improperly.
The syringes have a low dead space design, which means small amounts of liquid can remain in the syringe after drawing medication. This could cause inaccurate dosing if the user does not properly expel the liquid before administering the medication.
Users of CustomEyes Procedure Packs containing the specific syringes (Part Number 58000192) are affected. Healthcare professionals and patients using these packs for injections may be at risk of inaccurate dosing.
Check for the Part Number 58000192 on the syringe packaging. The recall includes CustomEyes Procedure Packs sold with these specific syringes, identified by the UDI-DI code 30886158009963 and Lot/Batch Number 6071161.
Look for the Part Number 58000192 on the syringe packaging to confirm if the product is affected.
The specific part number for the recalled syringes is 58000192.
Check for the Part Number 58000192 on the syringe packaging or look for the UDI-DI code 30886158009963 and Lot/Batch Number 6071161.
The recall does not require immediate stop use; check the packaging to confirm if your product is affected.
We’ve drafted a message you can send Beaver Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-2800-2024 — Beaver Visitec Beaver Visitec Hello, I own a Beaver Visitec that is covered by recall Z-2800-2024 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.
