Biopsybell recalls 10G Direct Single-Access needles with specific lot numbers due to potential unsterilized products. Affected items may pose infection risks if used without proper sterilization.
Products labeled as sterile were distributed, but may not have been sterilized.
Biopsybell is recalling certain 10G Direct Single-Access needles that may not have been properly sterilized. Using these needles without confirmed sterilization could lead to infection risks.
The needles were labeled as sterile but may not have been sterilized during manufacturing. This means they could be contaminated and cause infections if used without proper sterilization.
Healthcare professionals using the recalled needles for procedures are most at risk. Patients receiving procedures with these needles could face infection if not properly sterilized.
Check for the lot numbers: 2001201, 2003859, 20051288, or 20061419 on the needle packaging. The product is a 10G Direct Single-Access needle from Biopsybell.
Look for the lot numbers 2001201, 2003859, 20051288, or 20061419 on the needle packaging.
The needles may not have been properly sterilized, so they could pose an infection risk if used without confirmed sterilization.
Check the lot numbers on the packaging. If you have a recalled lot number, stop using them and contact Biopsybell for guidance.
Look for the lot numbers 2001201, 2003859, 20051288, or 20061419 on the needle packaging.
We’ve drafted a message you can send Biopsybell to request your refund or repair — edit it as you like.
Subject: Recall Z-1639-2021 — Biopsybell Biopsybell Hello, I own a Biopsybell that is covered by recall Z-1639-2021 from Biopsybell. 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.
