Vitreq recalls 25G blunt needles with luer-lock connector due to potential microscopic tears in sterile pouches, risking sterility compromise. All lots affected.
Microscopic tears of the sterile pouch may compromise sterility
Vitreq is recalling its 25G blunt needles with luer-lock connectors because tiny tears in the sterile packaging could compromise sterility. This means the needles might not be safe for medical use if the pouch is damaged.
Microscopic tears in the sterile pouch could allow contaminants to enter the needle packaging, potentially compromising sterility. This risk is specific to the packaging integrity during use.
Healthcare professionals using Vitreq 25G blunt needles with luer-lock connectors for medical procedures are affected. Patients receiving these needles could be at risk if the sterility is compromised.
Check for the product name 'VitreQ 25G Blunt Needles with luer-lock connector' and the reference number CN25.D05. All lots are affected, so no specific batch numbers are needed.
Identify the product by checking for the reference number CN25.D05 and the GTIN 8719214221645 on the packaging.
Yes, all lots of VitreQ 25G Blunt Needles with luer-lock connector (reference CN25.D05) are affected.
Look for the reference number CN25.D05 and GTIN 8719214221645 on the packaging. All lots are included in this recall.
The recall record does not specify a remedy, so no action is required beyond checking if your needles match the product description.
We’ve drafted a message you can send Vitreq Bv to request your refund or repair — edit it as you like.
Subject: Recall Z-0860-2020 — Vitreq Bv Vitreq Bv Hello, I own a Vitreq Bv that is covered by recall Z-0860-2020 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.