Biopsybell recalls 10G coaxial cannulas with Tuohy connection (code INTVM-CC) due to potential unsterilized products. Affected units may pose infection risk if used.
Products labeled as sterile were distributed, but may not have been sterilized.
Biopsybell is recalling 10G coaxial cannulas with Tuoh: connection (code INTVM-CC) because some products may not have been properly sterilized. Using unsterilized medical devices could lead to infections.
The products were labeled as sterile but may not have been sterilized during manufacturing. This could lead to infections if the cannulas are used in medical procedures without proper sterilization.
Medical professionals and patients who use the recalled cannulas for procedures. Those with the specific code INTVM-CC are most at risk.
Check for the product code INTVM-CC on the cannula packaging or label. The lot number 20102495 is also associated with this recall.
Look for the code INTVM-CC on the cannula packaging or label to confirm if it's affected.
The products were labeled as sterile but may not have been properly sterilized during manufacturing.
Check for the code INTVM-CC on the cannula packaging or label. The lot number 20102495 is also associated with this recall.
The recall 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-1648-2021 — Biopsybell Biopsybell Hello, I own a Biopsybell that is covered by recall Z-1648-2021 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.
