Biopsybell recalls 8G Direct Working Cannula Bevel Tips (code INTV-DWCB) 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 8:00mm cannula bevel tips with code INTV-DWCB because some were distributed without proper sterilization. Using unsterilized items could lead to infections.
The product was labeled as sterile but may not have been properly sterilized during manufacturing. This could result in unsterilized items being used, increasing infection risk during medical procedures.
Medical professionals and patients using these cannula tips for procedures. Those who have the specific lot number (30061432) are most at risk.
Check for the product code INTV-DWCB and lot number 30061432 on the cannula tips. These items were distributed by Biopsybell for medical use.
Look for the code INTV-DWCB and lot number 30061432 on the cannula tips.
The product was labeled as sterile but may not have been properly sterilized during manufacturing, posing infection risks if used.
Check for the code INTV-DWCB and lot number 30061432. If you have these items, contact Biopsybell for guidance.
The recall is for potential infection risk from unsterilized products, not a direct risk of serious injury.
We’ve drafted a message you can send Biopsybell to request your refund or repair — edit it as you like.
Subject: Recall Z-1645-2021 — Biopsybell Biopsybell Hello, I own a Biopsybell that is covered by recall Z-1645-2021 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.
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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.
