Vitreq Bv recalls 20G BF Blunt and Brush Needles due to potential microscopic tears in sterile pouches that could compromise sterility. Affected products include specific GTINs and all lots.
Microscopic tears of the sterile pouch may compromise sterility
Vitreq Bv is recalling two types of 20G BF needles because microscopic tears in their sterile packaging might compromise sterility. This could lead to infections if the needles are used without proper sterility.
The sterile pouches for these needles may develop microscopic tears during manufacturing or handling. If the pouch tears, the needles could become contaminated, increasing infection risk during medical procedures.
Medical professionals and surgical staff who use Vitreq 20G BF needles for procedures are most at risk. Patients using these needles could face infection if sterility is compromised.
Check for the product names 'VitreQ 20G BF Blunt Needles' (GTIN: 8719214221089) or 'VitreQ 20G BF Brush Needles' (GTIN: 8719214221102). All lots of these products are affected.
Identify the product by checking the GTIN numbers: 8719214221089 for blunt needles or 8719214221102 for brush needles.
The recall states that microscopic tears in the sterile pouch may compromise sterility, so they should not be used until the recall is addressed.
Check for the product names 'VitreQ 20G BF Blunt Needles' (GTIN: 8719214221089) or 'VitreQ 20G BF Brush Needles' (GTIN: 8719214221102). All lots are affected.
The recall does not specify a remedy, so contact Vitreq Bv directly for guidance on next steps.
We’ve drafted a message you can send Vitreq Bv to request your refund or repair — edit it as you like.
Subject: Recall Z-0848-2020 — Vitreq Bv Vitreq Bv Hello, I own a Vitreq Bv that is covered by recall Z-0848-2020 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.