Vitreq recalls 23G blunt needles with luer-lock connector due to potential microscopic pouch tears that could compromise sterility. All lots affected.
Microscopic tears of the sterile pouch may compromise sterility
Vitreq is recalling all 23G blunt needles with luer-lock connectors because tiny tears in the sterile pouch might make them unsafe. This could lead to infections if used improperly.
The sterile pouch may develop microscopic tears during use, which could compromise the needle's sterility. If the pouch isn't sterile, it might cause infections during medical procedures.
Users of VitreQ 23G blunt needles with luer-lock connectors are affected. Medical professionals and patients using these needles for procedures are most at risk.
Check for the product name 'VitreQ 23G Blunt Needles with luer-lock connector' and the reference number CN23.D05. All lots are affected.
Identify the product by checking for the reference number CN23.D05 and the GTIN 8719214221621.
Yes, all lots of VitreQ 23G blunt needles with luer-lock connector (reference CN23.D05) are affected.
Look for the reference number CN23.D05 and the GTIN 8719214221621 on the product packaging.
The recall does not require immediate stop use; check product details to confirm if affected.
We’ve drafted a message you can send Vitreq Bv to request your refund or repair — edit it as you like.
Subject: Recall Z-0859-2020 — Vitreq Bv Vitreq Bv Hello, I own a Vitreq Bv that is covered by recall Z-0859-2020 from Vitreq Bv. 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.
