Biopsybell recalls 11G Diamond Tip Cannula (code INTVMN-DWCD) due to potential unsterilized products. Affected items may not be sterile, posing infection risks. Contact for return instructions.
Products labeled as sterile were distributed, but may not have been sterilized.
Biopsybell is recalling 11G Diamond Tip Cannula products that may not have been properly sterilized. This could lead to infection risks for medical users if the items are used without proper sterility.
Products labeled as sterile were distributed but may not have been sterilized properly. This means the items could be contaminated and cause infections if used in medical procedures.
Medical professionals and patients using the recalled cannula for procedures. Those with the specific model code INTVMN-DWCD are most at risk.
Check for the model code INTVMN-DWCD on the product. The affected items were manufactured with lot number 2002437.
Look for the model code INTVMN-DWCD on the cannula to confirm if it's affected.
The products labeled as sterile may not have been properly sterilized, which could lead to infection risks during medical procedures.
Check for the model code INTVM:DWCD and lot number 2002437 on the product.
The recall record does not specify a remedy, so contact Biopsybell directly for guidance.
We’ve drafted a message you can send Biopsybell to request your refund or repair — edit it as you like.
Subject: Recall Z-1643-2021 — Biopsybell Biopsybell Hello, I own a Biopsybell that is covered by recall Z-1643-2021 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.
