Biopsybell recalls 10 gauge unilateral stylets with potential sterilization issues. Products may not have been properly sterilized, risking infection during medical procedures.
Products labeled as sterile were distributed, but may not have been sterilized.
Biopsybell is recalling 10-gauge direct unilateral stylets that may not have been properly sterilized. This could lead to infections if used in medical procedures.
The stylets were labeled as sterile but may not have been properly sterilized. This means they could cause infections during medical procedures if used without proper sterility.
Medical professionals who use these stylets for procedures may be affected. Patients using the recalled items face infection risks if the stylets are not sterile.
Check for the model code INTVM-DSSKBD on the stylet packaging. The lot numbers 19102741, 200127, 2001246, and 2101242 are associated with this recall.
Verify if the stylet has been properly sterilized by checking the lot number against the listed numbers.
The recall states that products labeled as sterile may not have been properly sterilized, so they are not safe for use without verification.
The recall does not specify a remedy, so check with the manufacturer for guidance on safe handling.
Look for the model code INTVM-DSSKBD and lot numbers 19102741, 200127, 2001246, or 2101242 on the packaging.
We’ve drafted a message you can send Biopsybell to request your refund or repair — edit it as you like.
Subject: Recall Z-1637-2021 — Biopsybell Biopsybell Hello, I own a Biopsybell that is covered by recall Z-1637-2021 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.
