Vitreq recalls 27G blunt needles with luer-lock connector due to potential pouch tears compromising sterility. All lots affected; no remedy specified.
Microscopic tears of the sterile pouch may compromise sterility
Vitreq is recalling all 27G blunt needles with luer-lock connectors (GTIN: 8719214221669) because microscopic tears in the sterile pouch could compromise sterility. This means the needles might not be safe for medical use if they cause contamination.
Microscopic tears in the sterile pouch could allow contamination, making the needles unsafe for medical procedures. This risk occurs during handling or use, but the needles themselves do not cause injury.
Medical professionals using these needles for procedures are affected. The risk is low since the hazard involves potential sterility compromise rather than immediate injury.
Check for the VitreQ 27G blunt needles with luer-lock connector (GTIN: 8719214221669). All lots are affected, so no specific batch numbers are needed.
Identify the product by the GTIN number 8719214221669 and the model CN27.D05.
The recall does not specify a stop-use action, so you can continue using them if they are still sterile.
The recall record does not mention any remedy or replacement options.
All lots of VitreQ 27G blunt needles with luer-lock connector (GTIN: 8719214221669) are affected.
We’ve drafted a message you can send Vitreq to request your refund or repair — edit it as you like.
Subject: Recall Z-0861-2020 — Vitreq Vitreq Hello, I own a Vitreq that is covered by recall Z-0861-2020 from Vitreq. 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.